bluedoor data·Job Postings API·bluedoor.sh ↗

Home › Companies › Iazuqy Fa Ocs Oraclecloud Com CX 1 › Clinical Research Coordinator Nephrology

Clinical Research Coordinator Nephrology

Iazuqy Fa Ocs Oraclecloud Com CX 1 · San Francisco, CA, United States; Millberry Union - FL 04 - RM E408, San Francisco, CA, US · Active · Oracle Recruiting Cloud / Fusion HCM

Job facts

FieldValue
CompanyIazuqy Fa Ocs Oraclecloud Com CX 1
TitleClinical Research Coordinator Nephrology
Normalized title-
Department / teamResearch and Laboratory
LocationSan Francisco, CA, United States
Work model-
Employment typeFull Time
Salary-
Statusactive
ATS providerOracle Recruiting Cloud / Fusion HCM
Posted / first seen2026-06-01 / 2026-06-02
Changed / last seen2026-06-06 / 2026-06-06

Related slices

PageWhat it containsOpen
Company jobsActive postings from Iazuqy Fa Ocs Oraclecloud Com CX 1.Open
Company breakdownsRole, location, ATS, and work model facets for this company.Open
ATS provider jobsActive postings observed through Oracle Recruiting Cloud / Fusion HCM.Open
Provider filtered searchThe same provider as a filtered job collection.Open
City jobsActive postings in San Francisco.Open
Department jobsActive postings in Research and Laboratory.Open
Lifecycle eventsOpen, update, close, and reopen events for this posting.Open
Original postingCanonical source or apply URL captured from the ATS.Open

Linked records

CompanyIazuqy Fa Ocs Oraclecloud Com CX 1
Source1ec01ec1-9ec0-4ca7-9242-3de42049e519
ATS providerOracle Recruiting Cloud / Fusion HCM

Description

Description The Clinical Research Coordinator (CRC) will perform independently or with general direction at the fully operational journey level of the series to execute, manage, and coordinate research protocols, as directed by the Clinical Research Supervisor and/or Principal Investigator (PI); may coordinate the data collection and operations of several concurrent clinical research studies under the guidelines of research protocols, UCSF and regulating agency policies. The CRC will coordinate various clinical studies on kidney disease patients. Duties include: enrolling patients in and assisting with execution of 1) industry trials for kidney disease; 2) enrollment of patients in biospecimen banking study from kidney disease clinic; 3) various smaller pilot studies in clinic 4) maintaining IRBs; and 5) other research studies as time permits. Responsibilities for all studies include: schedule patient visits and procedures; maintain accurate research charts and research study binders; perform accurate data collection and data entry; perform patient follow-up visits according to specific research study requirements; complete consent procedures and questionnaires with subjects; participate in research meetings; manage Investigator’s protocols in the Committee on Human Research (IRB) online system, as well as renewals and modifications of protocol applications and the implementation of new studies; participate in the review and writing of protocols to ensure institutional review board approval within University compliance; help assure compliance with all relevant regulatory agencies; oversee study data integrity; implement and maintain periodic quality control procedures; interface with departments to obtain UCSF approval prior to study initiation; maintain all regulatory documents; report study progress to investigators; participate in any internal and external audits or reviews of study protocols; and perform other duties as assigned. Also responsible for creating research accounts in Apex; linking patients to the research study and keeping their research status updated; linking encounters to the study and setting the research billing flag; creating lab orders and medication orders in Apex; scanning and uploading study consent forms into the patient’s medical chart; reviewing lab results, current medications, radiology studies, and providers’ progress notes for data collection into the research study database. The incumbent will also be required to create and maintain data entry accounts in Redcap and OnCore, the online data entry systems for research. Perform other duties as needed. There may be other opportunities to assist with other studies within the Division of Nephrology. If the incumbent is a certified phlebotomist, perform phlebotomy as needed. Responsibilities % of time Essential Function (Yes/No ) Key Responsibilities (To be completed by Supervisor) 50 Yes Study Coordination and Data Collection Identify subjects, develop recruitment and retention strategies, and screen and enroll study subjects. Schedule subjects for study visits; meet with them to administer questionnaires, collect medical history and perform study procedures. Maintain rapport and relationships with subjects to ensure effective communication and retention; respond to their diverse needs, schedule follow-up appointments, and become their intermediary; discuss study outcomes with providers to ensure continuity of care. Obtain informed consent; review information with subjects; assess and advocate for patient safety throughout each protocol procedure. Oversee subject reimbursement; work to resolve discrepancies and issues. Work with staff to ensure procedures are completed, specimens properly stored, and required data collected at visits; and ensure correct shipping and labeling measures. Coordinate, communicate and network with other studies and technicians to ensure scheduling efficiency; communicate with any affiliated groups. Conduct reviews of medical charts and electronic records to extract medical information and other data for use in studies. Implement needs assessments and recommendations for enhancements on patient coordination, data collection, data management, protocol adherence and study collaboration. Attend and actively participate in regular team meetings 20 Yes Data management and reporting of results Collect data during subject visits; enter data from visits, procedures, lab tests, and other subject-related participation into databases in a timely manner. Manage database structure for each protocol; update databases to improve data analysis and management; create new databases as needed. Create and maintain comprehensive data sets as requested by the CRC Supervisor and/or PI. Maintain data collection forms for effective data collection, entry, and analysis. Perform queries and analysis in databases. Work with Supervisor to maintain complete and accurate data in the study database; analyze the data as they become available. 5 Quality control procedures Oversee data integrity; initiate assessments of the adequacy of existing policies and procedures on subject recruitment, data collection, and data management. Update and maintain a procedure manual documenting all study-related procedures; help develop a plan to ensure consistency in data collection and data entry. Implement and maintain periodic quality control procedures Suggest modifications to the administrative infrastructure to accommodate increasing complexity of studies. Modify data collection instruments Maintain subject tracking systems. Arrange the exchange of and transport of specimens with collaborating Investigators and staff. Some specimen processing such as centrifugation, aliquoting, and shipping may be required in some studies Oversee the incoming data interpreted from samples and ensure that it is utilized correctly for analysis and publications. Ensure integrity and security of samples. If the incumbent is a certified phlebotomist, perform phlebotomy as needed. 5 Study Implementation 5 Specimen Management/ Maintenance 10 Protocol Submissions and Adherence Enter all existing and new study protocols into the Committee on Human Research (CHR) online system; seek assistance on maintaining all protocols in the system by communicating with CHR Analysts. Design and enhance case report forms and data collection forms as needed; provide manuscript feedback; continue to develop and maintain systems for assuring protocol adherence and data quality. Participate in the review and writing of protocols and related procedures to ensure institutional review board approval within University compliance. Renew, modify, and submit CHR applications and protocols; ensure that protocol applications are submitted in a timely manner; serve as a liaison between CHR and study Investigators. Provide quality assurance checks to note if protocols or UCSF CHR applications need to be modified; evaluate protocols on an ongoing basis and implement improvements as needed. 5 Regulatory responsibilities Assure studies are carried out according to Code of Federal Regulations, Good Clinical Practice, and UCSF regulations. Initiate and follow-up on CHR submissions and modifications; track approval status. Interface with departments to obtain UCSF approval prior to study initiation. Maintain regulatory documents; monitor timelines for data submission; document adverse events and submit to appropriate departments. Use sound judgment to maintain patient confidentiality when communicating with agencies, healthcare providers, other studies, and outside departments. Participate in and cooperate with any internal and external audits or reviews of study protocols; prepare necessary documentation. 100% (To update total %, enter the amount of time in whole numbers (without the % symbol - e.g., 15, 20) then highlight the total sum (e.g., 1%) at the bottom of the column and press F9. The total sum should add up to 100%.) Qualifications Required Qualifications HS graduation and sufficient experience and demonstrated skills to successfully perform the assigned duties and responsibilities; and/or equivalent experience/training. Attention to detail; strong interpersonal skills; excellent, effective verbal and written communication skills to coordinate with subjects, team members, other departments and outside institutions; and the ability to multi-task in a fast-paced environment while working with a diverse subject population Ability to work well independently, complete projects in a timely manner, and prioritize multiple projects to ensure the completion of essential tasks by deadlines. Preferred Qualifications Fluency in the usage of Committee of Human Research (CHR) online iRIS IRB system for submission, renewal, and modification of protocols through this system. Understanding of patient population to create rapport and a relationship, while also giving insight to what is realistic and appropriate for patient participation. Experience with electronic medical records. Phlebotomy certification Knowledge of UCSF and departmental policies for dealing with reimbursement, guidelines for research, confidentiality and HIPPA regulations, following the UCSF mission statement and purpose for research, and a clear understanding of policies and procedures on patient safety and confidentiality (electronic and hard copy medical records, patient charts, communication, etc.); knowledge of medical terminology, research policies and guidelines, guidelines for packing/shipping infectious substances, database building/analysis, and data management within some of the following: Access, Stata, SASS/ SPSS, and Teleform programming platforms Company About UCSF The University of California, San Francisco (UCSF) is a leading university dedicated to promoting health worldwide through advanced biomedical research, graduate-level education in the life sciences and health professions, and excellence in patient care. It is the only campus in the 10-campus UC system dedicated exclusively to the health sciences. We bring together the world’s leading experts in nearly every area of health. We are home to five Nobel laureates who have advanced the understanding of cancer, neurodegenerative diseases, aging and stem cells. Pride Values UCSF is a diverse community made of people with many skills and talents. We seek candidates whose work experience or community service has prepared them to contribute to our commitment to professionalism, respect, integrity, diversity and excellence – also known as our PRIDE values . In addition to our PRIDE values, UCSF is committed to equity – both in how we deliver care as well as our workforce. We are committed to building a broadly diverse community, nurturing a culture that is welcoming and supportive, and engaging diverse ideas for the provision of culturally competent education, discovery, and patient care. Additional information about UCSF is available here . Join us to find a rewarding career contributing to improving healthcare worldwide. Equal Employment Opportunity The University of California is an Equal Opportunity Employer. All qualified applicants will receive consideration for employment without regard to race, color, religion, sex, sexual orientation, gender identity, national origin, disability, age, protected veteran status, or other protected status under state or federal law. Salary Information The final salary and offer components are subject to additional approvals based on UC policy. Your placement within the salary range is dependent on a number of factors including your work experience and internal equity within this position classification at UCSF. For positions that are represented by a labor union, placement within the salary range will be guided by the rules in the collective bargaining agreement. To learn more about the benefits of working at UCSF, including total compensation, please visit: https://ucnet.universityofcalifornia.edu/compensation-and-benefits/index.html

Full job record

Job ID8a3d913b2efeaf4975e4f6d5f08b9b852dfd9c45
Org IDb73f2bf1-b0ab-47ed-8db1-1f14a038aa7c
Source ID1ec01ec1-9ec0-4ca7-9242-3de42049e519
Board ID1ec01ec1-9ec0-4ca7-9242-3de42049e519
Provideroracle_hcm
Provider Job Key2771
TitleClinical Research Coordinator Nephrology
Normalized Title—
Statusactive
Activeyes
Location TextSan Francisco, CA, United States; Millberry Union - FL 04 - RM E408, San Francisco, CA, US
DepartmentResearch and Laboratory
Team—
Employment Typefull_time
Workplace Type—
Remote Policy—
CountryUnited States
RegionCA
CitySan Francisco
Salary RawDescription The Clinical Research Coordinator (CRC) will perform independently or with general direction at the fully operational journey level of the series to execute, manage, and coordinate research protocols, as directed by the Clinical Research Supervisor and/or Principal Investigator (PI); may coordinate the data collection and operations of several concurrent clinical research studies under the guidelines of research protocols, UCSF and regulating agency policies. The CRC will coordinate various clinical studies on kidney disease patients. Duties include: enrolling patients in and assisting with execution of 1) industry trials for kidney disease; 2) enrollment of patients in biospecimen banking study from kidney disease clinic; 3) various smaller pilot studies in clinic 4) maintaining IRBs; and 5) other research studies as time permits. Responsibilities for all studies include: schedule patient visits and procedures; maintain accurate research charts and research study binders; perform accurate data collection and data entry; perform patient follow-up visits according to specific research study requirements; complete consent procedures and questionnaires with subjects; participate in research meetings; manage Investigator’s protocols in the Committee on Human Research (IRB) online system, as well as renewals and modifications of protocol applications and the implementation of new studies; participate in the review and writing of protocols to ensure institutional review board approval within University compliance; help assure compliance with all relevant regulatory agencies; oversee study data integrity; implement and maintain periodic quality control procedures; interface with departments to obtain UCSF approval prior to study initiation; maintain all regulatory documents; report study progress to investigators; participate in any internal and external audits or reviews of study protocols; and perform other duties as assigned. Also responsible for creating research accounts in Apex; linking patients to the research study and keeping their research status updated; linking encounters to the study and setting the research billing flag; creating lab orders and medication orders in Apex; scanning and uploading study consent forms into the patient’s medical chart; reviewing lab results, current medications, radiology studies, and providers’ progress notes for data collection into the research study database. The incumbent will also be required to create and maintain data entry accounts in Redcap and OnCore, the online data entry systems for research. Perform other duties as needed. There may be other opportunities to assist with other studies within the Division of Nephrology. If the incumbent is a certified phlebotomist, perform phlebotomy as needed. Responsibilities % of time Essential Function (Yes/No ) Key Responsibilities (To be completed by Supervisor) 50 Yes Study Coordination and Data Collection Identify subjects, develop recruitment and retention strategies, and screen and enroll study subjects. Schedule subjects for study visits; meet with them to administer questionnaires, collect medical history and perform study procedures. Maintain rapport and relationships with subjects to ensure effective communication and retention; respond to their diverse needs, schedule follow-up appointments, and become their intermediary; discuss study outcomes with providers to ensure continuity of care. Obtain informed consent; review information with subjects; assess and advocate for patient safety throughout each protocol procedure. Oversee subject reimbursement; work to resolve discrepancies and issues. Work with staff to ensure procedures are completed, specimens properly stored, and required data collected at visits; and ensure correct shipping and labeling measures. Coordinate, communicate and network with other studies and technicians to ensure scheduling efficiency; communicate with any affiliated groups. Conduct reviews of medical charts and electronic records to extract medical information and other data for use in studies. Implement needs assessments and recommendations for enhancements on patient coordination, data collection, data management, protocol adherence and study collaboration. Attend and actively participate in regular team meetings 20 Yes Data management and reporting of results Collect data during subject visits; enter data from visits, procedures, lab tests, and other subject-related participation into databases in a timely manner. Manage database structure for each protocol; update databases to improve data analysis and management; create new databases as needed. Create and maintain comprehensive data sets as requested by the CRC Supervisor and/or PI. Maintain data collection forms for effective data collection, entry, and analysis. Perform queries and analysis in databases. Work with Supervisor to maintain complete and accurate data in the study database; analyze the data as they become available. 5 Quality control procedures Oversee data integrity; initiate assessments of the adequacy of existing policies and procedures on subject recruitment, data collection, and data management. Update and maintain a procedure manual documenting all study-related procedures; help develop a plan to ensure consistency in data collection and data entry. Implement and maintain periodic quality control procedures Suggest modifications to the administrative infrastructure to accommodate increasing complexity of studies. Modify data collection instruments Maintain subject tracking systems. Arrange the exchange of and transport of specimens with collaborating Investigators and staff. Some specimen processing such as centrifugation, aliquoting, and shipping may be required in some studies Oversee the incoming data interpreted from samples and ensure that it is utilized correctly for analysis and publications. Ensure integrity and security of samples. If the incumbent is a certified phlebotomist, perform phlebotomy as needed. 5 Study Implementation 5 Specimen Management/ Maintenance 10 Protocol Submissions and Adherence Enter all existing and new study protocols into the Committee on Human Research (CHR) online system; seek assistance on maintaining all protocols in the system by communicating with CHR Analysts. Design and enhance case report forms and data collection forms as needed; provide manuscript feedback; continue to develop and maintain systems for assuring protocol adherence and data quality. Participate in the review and writing of protocols and related procedures to ensure institutional review board approval within University compliance. Renew, modify, and submit CHR applications and protocols; ensure that protocol applications are submitted in a timely manner; serve as a liaison between CHR and study Investigators. Provide quality assurance checks to note if protocols or UCSF CHR applications need to be modified; evaluate protocols on an ongoing basis and implement improvements as needed. 5 Regulatory responsibilities Assure studies are carried out according to Code of Federal Regulations, Good Clinical Practice, and UCSF regulations. Initiate and follow-up on CHR submissions and modifications; track approval status. Interface with departments to obtain UCSF approval prior to study initiation. Maintain regulatory documents; monitor timelines for data submission; document adverse events and submit to appropriate departments. Use sound judgment to maintain patient confidentiality when communicating with agencies, healthcare providers, other studies, and outside departments. Participate in and cooperate with any internal and external audits or reviews of study protocols; prepare necessary documentation. 100% (To update total %, enter the amount of time in whole numbers (without the % symbol - e.g., 15, 20) then highlight the total sum (e.g., 1%) at the bottom of the column and press F9. The total sum should add up to 100%.) Qualifications Required Qualifications HS graduation and sufficient experience and demonstrated skills to successfully perform the assigned duties and responsibilities; and/or equivalent experience/training. Attention to detail; strong interpersonal skills; excellent, effective verbal and written communication skills to coordinate with subjects, team members, other departments and outside institutions; and the ability to multi-task in a fast-paced environment while working with a diverse subject population Ability to work well independently, complete projects in a timely manner, and prioritize multiple projects to ensure the completion of essential tasks by deadlines. Preferred Qualifications Fluency in the usage of Committee of Human Research (CHR) online iRIS IRB system for submission, renewal, and modification of protocols through this system. Understanding of patient population to create rapport and a relationship, while also giving insight to what is realistic and appropriate for patient participation. Experience with electronic medical records. Phlebotomy certification Knowledge of UCSF and departmental policies for dealing with reimbursement, guidelines for research, confidentiality and HIPPA regulations, following the UCSF mission statement and purpose for research, and a clear understanding of policies and procedures on patient safety and confidentiality (electronic and hard copy medical records, patient charts, communication, etc.); knowledge of medical terminology, research policies and guidelines, guidelines for packing/shipping infectious substances, database building/analysis, and data management within some of the following: Access, Stata, SASS/ SPSS, and Teleform programming platforms Company About UCSF The University of California, San Francisco (UCSF) is a leading university dedicated to promoting health worldwide through advanced biomedical research, graduate-level education in the life sciences and health professions, and excellence in patient care. It is the only campus in the 10-campus UC system dedicated exclusively to the health sciences. We bring together the world’s leading experts in nearly every area of health. We are home to five Nobel laureates who have advanced the understanding of cancer, neurodegenerative diseases, aging and stem cells. Pride Values UCSF is a diverse community made of people with many skills and talents. We seek candidates whose work experience or community service has prepared them to contribute to our commitment to professionalism, respect, integrity, diversity and excellence – also known as our PRIDE values . In addition to our PRIDE values, UCSF is committed to equity – both in how we deliver care as well as our workforce. We are committed to building a broadly diverse community, nurturing a culture that is welcoming and supportive, and engaging diverse ideas for the provision of culturally competent education, discovery, and patient care. Additional information about UCSF is available here . Join us to find a rewarding career contributing to improving healthcare worldwide. Equal Employment Opportunity The University of California is an Equal Opportunity Employer. All qualified applicants will receive consideration for employment without regard to race, color, religion, sex, sexual orientation, gender identity, national origin, disability, age, protected veteran status, or other protected status under state or federal law. Salary Information The final salary and offer components are subject to additional approvals based on UC policy. Your placement within the salary range is dependent on a number of factors including your work experience and internal equity within this position classification at UCSF. For positions that are represented by a labor union, placement within the salary range will be guided by the rules in the collective bargaining agreement. To learn more about the benefits of working at UCSF, including total compensation, please visit: https://ucnet.universityofcalifornia.edu/compensation-and-benefits/index.html
Salary Min—
Salary Max—
Salary Currency—
Salary Period—
Source URLhttps://iazuqy.fa.ocs.oraclecloud.com/hcmUI/CandidateExperience/en/sites/CX_1/job/2771
Apply URLhttps://iazuqy.fa.ocs.oraclecloud.com/hcmUI/CandidateExperience/en/sites/CX_1/job/2771
First Seen At2026-06-02 11:37:10Z
Last Seen At2026-06-06 19:36:14Z
Last Checked At2026-06-06 19:36:14Z
Last Changed At2026-06-06 11:18:11Z
Inactive At—
Source Posted At2026-06-01 00:00:00Z
Source Updated At—
Raw Payload Uris3://job-postings-prod-raw-590183727216/raw/provider=oracle_hcm/board=iazuqy.fa.ocs.oraclecloud.com|CX_1/date=2026-06-06/2026-06-06T19-34-57-721Z-59ddc5abcdf6a871a8f8be65341758988893a47757f1c9e6ac5fa33dd96c8fbc.json
Event Fields
{
  "content_hash": "6699f9b3d081680a10a6263f128222cf0b58ecc88eb040ce63d621750eae1e8a",
  "source_hash": "e48a6cbaa6e724ea4d30a2908d000ed56d6e6cc2f1158a9917d79a630e69e406",
  "last_changed_at": "2026-06-06T11:18:11.556Z",
  "active_status": "active"
}
Parsed Structured
{
  "language": "en",
  "location": {
    "raw": "San Francisco, CA, United States",
    "city": "San Francisco",
    "region": "CA",
    "country": "United States",
    "is_remote": false,
    "confidence": 0.8
  },
  "salary_max": null,
  "salary_min": null,
  "inferred_at": "2026-06-06T19:36:13.325Z",
  "launch_scope": {
    "reason": "english_us_canada",
    "included": true,
    "language": "en",
    "location": {
      "raw": "San Francisco, CA, United States",
      "city": "San Francisco",
      "region": "CA",
      "country": "United States",
      "is_remote": false,
      "confidence": 0.8
    },
    "countries": [
      "United States"
    ]
  },
  "remote_policy": null,
  "salary_period": null,
  "workplace_type": null,
  "salary_currency": null
}
Extensions
{}
Native Structured
{
  "detail": {
    "Id": "2771",
    "Title": "Clinical Research Coordinator Nephrology",
    "media": [],
    "skills": [],
    "JobType": null,
    "Category": "Research and Laboratory",
    "JobGrade": null,
    "JobLevel": null,
    "JobShift": "Day",
    "WorkDays": null,
    "WorkHours": null,
    "WorkYears": null,
    "Department": null,
    "HotJobFlag": false,
    "StudyLevel": "High School Graduate",
    "WorkMonths": null,
    "WorkerType": null,
    "GeographyId": 100000008360352,
    "JobFamilyId": 300000008226025,
    "JobFunction": "Clinical Research Human Subj",
    "JobSchedule": "Full time",
    "BusinessUnit": null,
    "ContractType": null,
    "Organization": null,
    "TrendingFlag": true,
    "workLocation": [
      {
        "Country": "US",
        "Region1": "San Francisco",
        "Region2": "CA",
        "Region3": null,
        "Building": null,
        "Latitude": "37.76957",
        "Longitude": "-122.44356",
        "LocationId": 300000009343061,
        "PostalCode": "94117",
        "TownOrCity": "San Francisco",
        "AddressLine1": "500 Parnassus Avenue",
        "AddressLine2": "Millberry Union",
        "AddressLine3": "E408",
        "AddressLine4": null,
        "LocationName": "Millberry Union - FL 04 - RM E408"
      }
    ],
    "ContentLocale": "en",
    "HiringManager": null,
    "LegalEmployer": null,
    "RequisitionId": 300000146936683,
    "WorkplaceType": "",
    "BusinessUnitId": 300000007556001,
    "OrganizationId": 300000007556001,
    "GeographyNodeId": 100000129729281,
    "JobFunctionCode": "211",
    "LegalEmployerId": 300000007380777,
    "PrimaryLocation": "San Francisco, CA, United States",
    "RequisitionType": "Openly Recruited",
    "NumberOfOpenings": null,
    "WorkplaceTypeCode": null,
    "BeFirstToApplyFlag": false,
    "otherWorkLocations": [],
    "secondaryLocations": [],
    "ExternalContactName": null,
    "ShortDescriptionStr": "",
    "ExternalContactEmail": null,
    "ExternalPostedEndDate": null,
    "OtherRequisitionTitle": null,
    "requisitionFlexFields": [
      {
        "Value": "4 hours",
        "Prompt": "Shift Length",
        "ControlType": "SingleChoiceList",
        "SequenceNumber": 4
      },
      {
        "Value": "80000.00",
        "Prompt": "Budgeted Job Salary Range",
        "ControlType": "TextArea",
        "SequenceNumber": 7
      },
      {
        "Value": "Parnassus Heights (SF)",
        "Prompt": "Campus Location 1",
        "ControlType": "SingleChoiceList",
        "SequenceNumber": 8
      },
      {
        "Value": "RX",
        "Prompt": "Bargaining Unit",
        "ControlType": "SingleChoiceList",
        "SequenceNumber": 11
      },
      {
        "Value": "Limited Appt",
        "Prompt": "Employee Class",
        "ControlType": "SingleChoiceList",
        "SequenceNumber": 13
      },
      {
        "Value": "Non-exempt",
        "Prompt": "FLSA Status",
        "ControlType": "SingleChoiceList",
        "SequenceNumber": 14
      },
      {
        "Value": "009335 | CLIN RSCH CRD",
        "Prompt": "Job Code and Payroll Title",
        "ControlType": "SingleChoiceList",
        "SequenceNumber": 19
      },
      {
        "Value": "Fully On-Site",
        "Prompt": "Workplace",
        "ControlType": "SingleChoiceList",
        "SequenceNumber": 20
      },
      {
        "Value": "50",
        "Prompt": "FTE%",
        "ControlType": "TextArea",
        "SequenceNumber": 28
      }
    ],
    "ApplyWhenNotPostedFlag": true,
    "DomesticTravelRequired": null,
    "ExternalDescriptionStr": "<p>The Clinical Research Coordinator (CRC) will perform independently or with general direction at the fully operational journey level of the series to execute, manage, and coordinate research protocols, as directed by the Clinical Research Supervisor and/or Principal Investigator (PI); may coordinate the data collection and operations of several concurrent clinical research studies under the guidelines of research protocols, UCSF and regulating agency policies.</p><p>The CRC will coordinate various clinical studies on kidney disease patients. Duties include: enrolling patients in and assisting with execution of 1) industry trials for kidney disease; 2) enrollment of patients in biospecimen banking study from kidney disease clinic; 3) various smaller pilot studies in clinic 4) maintaining IRBs; and 5) other research studies as time permits. Responsibilities for all studies include: schedule patient visits and procedures; maintain accurate research charts and research study binders; perform accurate data collection and data entry; perform patient follow-up visits according to specific research study requirements; complete consent procedures and questionnaires with subjects; participate in research meetings; manage Investigator’s protocols in the Committee on Human Research (IRB) online system, as well as renewals and modifications of protocol applications and the implementation of new studies; participate in the review and writing of protocols to ensure institutional review board approval within University compliance; help assure compliance with all relevant regulatory agencies; oversee study data integrity; implement and maintain periodic quality control procedures; interface with departments to obtain UCSF approval prior to study initiation; maintain all regulatory documents; report study progress to investigators; participate in any internal and external audits or reviews of study protocols; and perform other duties as assigned. &nbsp;Also responsible for creating research accounts in Apex; linking patients to the research study and keeping their research status updated; linking encounters to the study and setting the research billing flag; creating lab orders and medication orders in Apex; scanning and uploading study consent forms into the patient’s medical chart; reviewing lab results, current medications, radiology studies, and providers’ progress notes for data collection into the research study database. The incumbent will also be required to create and maintain data entry accounts in Redcap and OnCore, the online data entry systems for research. Perform other duties as needed. There may be other opportunities to assist with other studies within the Division of Nephrology. &nbsp;If the incumbent is a certified phlebotomist, perform phlebotomy as needed. &nbsp;</p>",
    "ObjectVerNumberProfile": "6",
    "PrimaryLocationCountry": "US",
    "CorporateDescriptionStr": "<div>\n <b>About UCSF</b>\n</div>\n<div>\n <br>\n</div>\n<div>\n The University of California, San Francisco (UCSF) is a leading university dedicated to promoting health worldwide through advanced biomedical research, graduate-level education in the life sciences and health professions, and excellence in patient care. It is the only campus in the 10-campus UC system dedicated exclusively to the health sciences. We bring together the world’s leading experts in nearly every area of health. We are home to five Nobel laureates who have advanced the understanding of cancer, neurodegenerative diseases, aging and stem cells.\n</div>\n<div>\n <br>\n</div>\n<div>\n <b>Pride Values</b>\n</div>\n<div>\n <br>\n</div>\n<div>\n UCSF is a diverse community made of people with many skills and talents. We seek candidates whose work experience or community service has prepared them to contribute to our commitment to professionalism, respect, integrity, diversity and excellence – also known as <a href=\"https://www.ucsf.edu/about/mission-and-values\" target=\"_blank\" rel=\"nofollow\">our PRIDE values</a>.\n</div>\n<div>\n <br>\n</div>\n<div>\n In addition to our PRIDE values, UCSF is committed to equity – both in how we deliver care as well as our workforce. We are committed to building a broadly diverse community, nurturing a culture that is welcoming and supportive, and engaging diverse ideas for the provision of culturally competent education, discovery, and patient care. Additional information about UCSF is available <a href=\"https://diversity.ucsf.edu/\" target=\"_blank\" rel=\"nofollow\">here</a>.\n</div>\n<div>\n <br>\n</div>\n<div>\n Join us to find a rewarding career contributing to improving healthcare worldwide.\n</div>\n<div>\n <b><br></b>\n</div>\n<div>\n <b>Equal Employment Opportunity</b>\n</div>\n<div>\n <br>\n</div>\n<div>\n <i>The University of California is an Equal Opportunity Employer. All qualified applicants will receive consideration for employment without regard to race, color, religion, sex, sexual orientation, gender identity, national origin, disability, age, protected veteran status, or other protected status under state or federal law.</i>\n</div>\n<div>\n <i><br></i>\n</div>\n<div>\n <div>\n  <b>Salary Information</b>\n </div>\n <div>\n  <br>\n </div>\n <div>\n  The final salary and offer components are subject to additional approvals based on UC policy.\n </div>\n <div>\n  <br>\n </div>\n <div>\n  Your placement within the salary range is dependent on a number of factors including your work experience and internal equity within this position classification at UCSF. For positions that are represented by a labor union, placement within the salary range will be guided by the rules in the collective bargaining agreement.\n </div>\n <div>\n  <br>\n </div>\n <div>\n  To learn more about the benefits of working at UCSF, including total compensation, please visit: <a href=\"https://nam10.safelinks.protection.outlook.com/?url=https%3A%2F%2Furldefense.com%2Fv3%2F__https%3A%2Fucnet.universityofcalifornia.edu%2Fcompensation-and-benefits%2Findex.html__%3B!!LQC6Cpwp!uPLWUNVR0rFXMaSxiegp2raBmrA8C98l3-u68X5cON0um3OJMU_XUivT5BcOsGRYxtGPmgcRECZCCPoE3BWZz30_aN1A%24&amp;data=05%7C02%7Ckellestad%40deloitte.com%7C09196a31acf74487ae9208de8b4b632a%7C36da45f1dd2c4d1faf135abe46b99921%7C0%7C0%7C639101353128138525%7CUnknown%7CTWFpbGZsb3d8eyJFbXB0eU1hcGkiOnRydWUsIlYiOiIwLjAuMDAwMCIsIlAiOiJXaW4zMiIsIkFOIjoiTWFpbCIsIldUIjoyfQ%3D%3D%7C0%7C%7C%7C&amp;sdata=YCGJ3ybBxqEKRAZBHus2KaGkepN2dmG3pACwRBxDLng%3D&amp;reserved=0\" target=\"_blank\" rel=\"nofollow\">https://ucnet.universityofcalifornia.edu/compensation-and-benefits/index.html</a>\n </div>\n <div style=\"font-style:italic\">\n  <br>\n </div>\n</div>",
    "ExternalPostedStartDate": null,
    "ExternalQualificationsStr": "<p><strong>Required Qualifications</strong></p><ul><li>HS graduation and sufficient experience and demonstrated skills to successfully perform the assigned duties and responsibilities; and/or equivalent experience/training.&nbsp;</li><li>Attention to detail; strong interpersonal skills; excellent, effective verbal and written communication skills to coordinate with subjects, team members, other departments and outside institutions; and the ability to multi-task in a fast-paced environment while working with a diverse subject population</li><li>Ability to work well independently, complete projects in a timely manner, and prioritize multiple projects to ensure the completion of essential tasks by deadlines.</li></ul><p>&nbsp;</p><p><strong>Preferred Qualifications</strong></p><ul><li>Fluency in the usage of Committee of Human Research (CHR) online iRIS IRB system for submission, renewal, and modification of protocols through this system.</li><li>Understanding of patient population to create rapport and a relationship, while also giving insight to what is realistic and appropriate for patient participation.</li><li>Experience with electronic medical records.</li><li>Phlebotomy certification</li><li><p>Knowledge of UCSF and departmental policies for dealing with reimbursement, guidelines for research, confidentiality and HIPPA regulations, following the UCSF mission statement and purpose for research, and a clear understanding of policies and procedures on patient safety and confidentiality (electronic and hard copy medical records, patient charts, communication, etc.); knowledge of medical terminology, research policies and guidelines, guidelines for packing/shipping infectious substances, database building/analysis, and data management within some of the following:&nbsp; Access, Stata, SASS/ SPSS, and Teleform programming platforms</p><p>&nbsp;</p></li></ul>",
    "InternalQualificationsStr": "<p><strong>Required Qualifications</strong></p><ul><li>HS graduation and sufficient experience and demonstrated skills to successfully perform the assigned duties and responsibilities; and/or equivalent experience/training.&nbsp;</li><li>Attention to detail; strong interpersonal skills; excellent, effective verbal and written communication skills to coordinate with subjects, team members, other departments and outside institutions; and the ability to multi-task in a fast-paced environment while working with a diverse subject population</li><li>Ability to work well independently, complete projects in a timely manner, and prioritize multiple projects to ensure the completion of essential tasks by deadlines.</li></ul><p>&nbsp;</p><p><strong>Preferred Qualifications</strong></p><ul><li>Fluency in the usage of Committee of Human Research (CHR) online iRIS IRB system for submission, renewal, and modification of protocols through this system.</li><li>Understanding of patient population to create rapport and a relationship, while also giving insight to what is realistic and appropriate for patient participation.</li><li>Experience with electronic medical records.</li><li>Phlebotomy certification</li><li><p>Knowledge of UCSF and departmental policies for dealing with reimbursement, guidelines for research, confidentiality and HIPPA regulations, following the UCSF mission statement and purpose for research, and a clear understanding of policies and procedures on patient safety and confidentiality (electronic and hard copy medical records, patient charts, communication, etc.); knowledge of medical terminology, research policies and guidelines, guidelines for packing/shipping infectious substances, database building/analysis, and data management within some of the following:&nbsp; Access, Stata, SASS/ SPSS, and Teleform programming platforms</p><p>&nbsp;</p></li></ul>",
    "OrganizationDescriptionStr": "",
    "primaryLocationCoordinates": [
      {
        "Latitude": "37.77712",
        "Longitude": "-122.41966",
        "CountryCode": "US",
        "GeographyId": 100000008360352,
        "GeographyNodeId": 100000129729281
      }
    ],
    "ExternalResponsibilitiesStr": "<p style=\"text-align: justify;\">&nbsp;</p><figure class=\"table\"><table border=\"0\" cellspacing=\"0\" cellpadding=\"0\" width=\"699\" style=\"border-collapse: collapse; width: 524.6pt;\"><tbody><tr><td width=\"83\" valign=\"top\" style=\"border: 1pt solid windowtext; padding: 0in 5.4pt; width: 61.9pt;\"><p style=\"text-align: center;\">%&nbsp;</p><p style=\"text-align: center;\"><strong>of time</strong></p></td><td width=\"70\" style=\"border: 1pt solid windowtext; padding: 0in 5.4pt; width: 52.85pt;\"><p style=\"text-align: center;\"><span style=\"font-size: 7pt;\"><strong>Essential Function (Yes/No</strong>)</span></p></td><td width=\"546\" valign=\"top\" style=\"border: 1pt solid windowtext; padding: 0in 5.4pt; width: 409.85pt;\"><p style=\"text-align: center;\"><span style=\"font-size: 9pt;\"><strong>&nbsp;</strong></span>&nbsp;</p><p style=\"text-align: center;\"><span style=\"font-size: 9pt;\"><strong>Key Responsibilities</strong></span></p><p style=\"text-align: center;\"><i><span style=\"font-size: 9pt;\"><strong>(To be completed by Supervisor)</strong></span></i></p></td></tr><tr><td width=\"83\" valign=\"top\" style=\"border-width: medium 1pt 1pt; border-style: none dotted solid; border-color: currentcolor windowtext windowtext; padding: 0in 5.4pt; width: 61.9pt;\"><p style=\"text-align: center;\">50</p></td><td width=\"70\" valign=\"top\" style=\"border-width: medium 1pt 1pt medium; border-style: none dotted dotted none; border-color: currentcolor windowtext windowtext currentcolor; padding: 0in 5.4pt; width: 52.85pt;\">Yes</td><td width=\"546\" valign=\"top\" style=\"border-width: medium 1pt 1pt medium; border-style: none dotted dotted none; border-color: currentcolor windowtext windowtext currentcolor; padding: 0in 5.4pt; width: 409.85pt;\"><figure class=\"table\"><table border=\"0\" cellspacing=\"0\" cellpadding=\"0\" style=\"border-collapse: collapse;\"><tbody><tr><td valign=\"top\" style=\"border: 1pt dotted rgb(170, 170, 170); padding: 0in 5.25pt;\"><h3 style=\"margin: 0in;\"><span style=\"color: black; font-family: Arial, sans-serif;\"><i><span style=\"font-size: 10pt; font-weight: normal;\">Study Coordination and Data Collection</span></i></span></h3><ul style=\"list-style-type: disc;\"><li style=\"color: black; vertical-align: baseline;\">Identify subjects, develop recruitment and retention strategies, and screen and enroll study subjects.</li><li style=\"color: black; vertical-align: baseline;\">Schedule subjects for study visits; meet with them to administer questionnaires, collect medical history<span style=\"font-size: 11pt;\">&nbsp;</span>and perform study procedures.</li><li style=\"color: black; vertical-align: baseline;\">Maintain rapport and relationships with subjects to ensure effective communication and retention; respond to their diverse needs, schedule follow-up appointments, and become their intermediary; discuss study outcomes with providers to ensure continuity of care.</li><li style=\"color: black; vertical-align: baseline;\">Obtain informed consent; review information with subjects; assess and advocate for patient safety throughout each protocol procedure.</li><li style=\"color: black; vertical-align: baseline;\">Oversee subject reimbursement; work to resolve discrepancies and issues.<span>&nbsp; &nbsp; &nbsp; &nbsp; &nbsp;</span></li><li style=\"color: black; vertical-align: baseline;\">Work with staff to ensure procedures are completed, specimens properly stored, and required data collected at visits; and ensure correct shipping and labeling measures.</li><li style=\"color: black; vertical-align: baseline;\">Coordinate, communicate and network with other studies and technicians to ensure scheduling efficiency; communicate with any affiliated groups.</li><li style=\"color: black; vertical-align: baseline;\">Conduct reviews of medical charts and electronic records to extract medical information and other data for use in studies.</li><li style=\"color: black; vertical-align: baseline;\">Implement needs assessments and recommendations for enhancements on patient coordination, data collection, data management, protocol adherence and study collaboration.</li><li style=\"color: black; vertical-align: baseline;\">Attend and actively participate in regular team meetings</li></ul><p style=\"margin-left: 0.5in; vertical-align: baseline;\">&nbsp;</p></td></tr></tbody></table></figure><p>&nbsp;</p></td></tr><tr><td width=\"83\" valign=\"top\" style=\"border-width: medium 1pt 1pt; border-style: none dotted solid; border-color: currentcolor windowtext windowtext; padding: 0in 5.4pt; width: 61.9pt;\"><p style=\"text-align: center;\">20</p><p>&nbsp;</p></td><td width=\"70\" valign=\"top\" style=\"border-width: medium 1pt 1pt medium; border-style: none dotted dotted none; border-color: currentcolor windowtext windowtext currentcolor; padding: 0in 5.4pt; width: 52.85pt;\">Yes</td><td width=\"546\" valign=\"top\" style=\"border-width: medium 1pt 1pt medium; border-style: none dotted dotted none; border-color: currentcolor windowtext windowtext currentcolor; padding: 0in 5.4pt; width: 409.85pt;\"><figure class=\"table\"><table border=\"0\" cellspacing=\"0\" cellpadding=\"0\" style=\"border-collapse: collapse;\"><tbody><tr><td valign=\"top\" style=\"border: 1pt dotted rgb(170, 170, 170); padding: 0in 5.25pt;\"><h3 style=\"margin: 0in;\"><span style=\"color: black; font-family: Arial, sans-serif;\"><i><span style=\"font-size: 10pt; font-weight: normal;\">Data management and reporting of results</span></i></span></h3><ul style=\"list-style-type: disc;\"><li style=\"color: black; vertical-align: baseline;\">Collect data during subject visits; enter data from visits, procedures, lab tests, and other subject-related participation into databases in a timely manner.</li><li style=\"color: black; vertical-align: baseline;\">Manage database structure for each protocol; update databases to improve data analysis and management; create new databases as needed.</li><li style=\"color: black; vertical-align: baseline;\">Create and maintain comprehensive data sets as requested by the CRC Supervisor and/or PI. &nbsp;</li><li style=\"color: black; vertical-align: baseline;\">Maintain data collection forms for effective data collection, entry, and analysis. &nbsp;</li><li style=\"color: black; vertical-align: baseline;\">Perform queries and analysis in databases.</li><li style=\"color: black; vertical-align: baseline;\">Work with Supervisor to maintain complete and accurate data in the study database; analyze the data as they become available.</li></ul><p style=\"margin-left: 0.5in; vertical-align: baseline;\">&nbsp;</p></td></tr></tbody></table></figure><p>&nbsp;</p></td></tr><tr><td width=\"83\" valign=\"top\" style=\"border-width: medium 1pt 1pt; border-style: none dotted solid; border-color: currentcolor windowtext windowtext; padding: 0in 5.4pt; width: 61.9pt;\"><p style=\"text-align: center;\">5</p></td><td width=\"70\" valign=\"top\" style=\"border-width: medium 1pt 1pt medium; border-style: none dotted dotted none; border-color: currentcolor windowtext windowtext currentcolor; padding: 0in 5.4pt; width: 52.85pt;\">&nbsp;</td><td width=\"546\" valign=\"top\" style=\"border-width: medium 1pt 1pt medium; border-style: none dotted dotted none; border-color: currentcolor windowtext windowtext currentcolor; padding: 0in 5.4pt; width: 409.85pt;\"><p><span style=\"color: black;\"><i>Quality control procedures&nbsp;</i></span></p><ul style=\"list-style-type: disc;\"><li style=\"color: black; vertical-align: baseline;\">Oversee data&nbsp;integrity; initiate assessments of the adequacy of existing policies and procedures on subject recruitment, data collection, and data management. &nbsp;</li><li style=\"color: black; vertical-align: baseline;\">Update and maintain a procedure manual documenting all study-related procedures; help develop a plan to ensure consistency in data collection and data entry.</li><li style=\"color: black; vertical-align: baseline;\">Implement and maintain periodic quality control procedures</li><li style=\"color: black; vertical-align: baseline;\">Suggest modifications to the administrative infrastructure to accommodate increasing complexity of studies. &nbsp;</li><li style=\"color: black; vertical-align: baseline;\">Modify data collection instruments</li><li style=\"color: black; vertical-align: baseline;\">Maintain subject tracking systems.</li><li style=\"color: black; vertical-align: baseline;\">Arrange the exchange of and transport of specimens with collaborating Investigators and staff.</li><li style=\"color: black; vertical-align: baseline;\">Some specimen processing such as centrifugation, aliquoting, and shipping may be required in some studies</li><li style=\"color: black; vertical-align: baseline;\">Oversee the incoming data interpreted from samples and ensure that it is utilized correctly for analysis and publications.</li><li style=\"color: black; vertical-align: baseline;\">Ensure integrity and security of samples.</li><li style=\"color: black;\">If the incumbent is a certified phlebotomist, perform phlebotomy as needed.<span>&nbsp;</span></li></ul></td></tr><tr><td width=\"83\" valign=\"top\" style=\"border-width: medium 1pt 1pt; border-style: none dotted solid; border-color: currentcolor windowtext windowtext; padding: 0in 5.4pt; width: 61.9pt;\"><p style=\"text-align: center;\">5</p></td><td width=\"70\" valign=\"top\" style=\"border-width: medium 1pt 1pt medium; border-style: none dotted dotted none; border-color: currentcolor windowtext windowtext currentcolor; padding: 0in 5.4pt; width: 52.85pt;\">&nbsp;</td><td width=\"546\" valign=\"top\" style=\"border-width: medium 1pt 1pt medium; border-style: none dotted dotted none; border-color: currentcolor windowtext windowtext currentcolor; padding: 0in 5.4pt; width: 409.85pt;\"><figure class=\"table\"><table border=\"0\" cellspacing=\"0\" cellpadding=\"0\" style=\"border-collapse: collapse;\"><tbody><tr><td valign=\"top\" style=\"border: 1pt dotted rgb(170, 170, 170); padding: 0in 5.25pt;\"><h3 style=\"margin: 0in;\"><span style=\"color: black; font-family: Arial, sans-serif;\"><i><span style=\"font-size: 10pt; font-weight: normal;\">Study Implementation</span></i></span></h3><p style=\"margin-left: 0.5in; vertical-align: baseline;\">&nbsp;</p></td></tr></tbody></table></figure><p>&nbsp;</p></td></tr><tr><td width=\"83\" valign=\"top\" style=\"border-width: medium 1pt 1pt; border-style: none dotted solid; border-color: currentcolor windowtext windowtext; padding: 0in 5.4pt; width: 61.9pt;\"><p style=\"text-align: center;\">5</p></td><td width=\"70\" valign=\"top\" style=\"border-width: medium 1pt 1pt medium; border-style: none dotted dotted none; border-color: currentcolor windowtext windowtext currentcolor; padding: 0in 5.4pt; width: 52.85pt;\">&nbsp;</td><td width=\"546\" valign=\"top\" style=\"border-width: medium 1pt 1pt medium; border-style: none dotted dotted none; border-color: currentcolor windowtext windowtext currentcolor; padding: 0in 5.4pt; width: 409.85pt;\"><figure class=\"table\"><table border=\"0\" cellspacing=\"0\" cellpadding=\"0\" style=\"border-collapse: collapse;\"><tbody><tr><td valign=\"top\" style=\"border: 1pt dotted rgb(170, 170, 170); padding: 0in 5.25pt;\"><h3 style=\"margin: 0in;\"><span style=\"color: black; font-family: Arial, sans-serif;\"><i><span style=\"font-size: 10pt; font-weight: normal;\">Specimen Management/ Maintenance</span></i></span></h3><p style=\"margin-left: 0.5in; vertical-align: baseline;\">&nbsp;</p></td></tr></tbody></table></figure><p>&nbsp;</p></td></tr><tr><td width=\"83\" valign=\"top\" style=\"border-width: medium 1pt 1pt; border-style: none dotted solid; border-color: currentcolor windowtext windowtext; padding: 0in 5.4pt; width: 61.9pt;\"><p style=\"text-align: center;\">10</p></td><td width=\"70\" valign=\"top\" style=\"border-width: medium 1pt 1pt medium; border-style: none dotted dotted none; border-color: currentcolor windowtext windowtext currentcolor; padding: 0in 5.4pt; width: 52.85pt;\">&nbsp;</td><td width=\"546\" valign=\"top\" style=\"border-width: medium 1pt 1pt medium; border-style: none dotted dotted none; border-color: currentcolor windowtext windowtext currentcolor; padding: 0in 5.4pt; width: 409.85pt;\"><p><span style=\"color: black;\"><i>Protocol Submissions and Adherence</i></span></p><ul style=\"list-style-type: disc;\"><li style=\"color: black; vertical-align: baseline;\">Enter all existing and new study protocols into the Committee on Human Research (CHR) online system; seek assistance on maintaining all protocols in the system by communicating with CHR Analysts.</li><li style=\"color: black; vertical-align: baseline;\">Design and enhance case report forms and data collection forms as needed; provide manuscript feedback; continue to develop and maintain systems for assuring protocol adherence and data quality.</li><li style=\"color: black; vertical-align: baseline;\">Participate in the review and writing of protocols and related procedures to ensure institutional review board approval within University compliance.</li><li style=\"color: black; vertical-align: baseline;\">Renew, modify, and submit CHR applications and protocols; ensure that protocol applications are submitted in a timely manner; serve as a liaison between CHR and study Investigators.</li><li style=\"color: black; vertical-align: baseline;\">Provide quality assurance checks to note if protocols or UCSF CHR applications need to be modified; evaluate protocols on an ongoing basis and implement improvements as needed.</li></ul></td></tr><tr><td width=\"83\" valign=\"top\" style=\"border-width: medium 1pt 1pt; border-style: none dotted solid; border-color: currentcolor windowtext windowtext; padding: 0in 5.4pt; width: 61.9pt;\"><p style=\"text-align: center;\">5</p></td><td width=\"70\" valign=\"top\" style=\"border-width: medium 1pt 1pt medium; border-style: none dotted dotted none; border-color: currentcolor windowtext windowtext currentcolor; padding: 0in 5.4pt; width: 52.85pt;\">&nbsp;</td><td width=\"546\" valign=\"top\" style=\"border-width: medium 1pt 1pt medium; border-style: none dotted dotted none; border-color: currentcolor windowtext windowtext currentcolor; padding: 0in 5.4pt; width: 409.85pt;\"><figure class=\"table\"><table border=\"0\" cellspacing=\"0\" cellpadding=\"0\" style=\"border-collapse: collapse;\"><tbody><tr><td valign=\"top\" style=\"border: 1pt dotted rgb(170, 170, 170); padding: 0in 5.25pt;\"><h3 style=\"margin: 0in;\"><span style=\"color: black; font-family: Arial, sans-serif;\"><i><span style=\"font-size: 10pt; font-weight: normal;\">Regulatory responsibilities</span></i></span></h3><ul style=\"list-style-type: disc;\"><li style=\"color: black; vertical-align: baseline;\">Assure studies are carried out according to Code of Federal Regulations, Good Clinical Practice, and UCSF regulations.</li><li style=\"color: black; vertical-align: baseline;\">Initiate and follow-up on CHR submissions and modifications; track approval status.</li><li style=\"color: black; vertical-align: baseline;\">Interface with departments to obtain UCSF approval prior to study initiation.</li><li style=\"color: black; vertical-align: baseline;\">Maintain regulatory documents; monitor timelines for data submission; document adverse events and submit to appropriate departments.</li><li style=\"color: black; vertical-align: baseline;\">Use sound judgment to maintain patient confidentiality when communicating with agencies, healthcare providers, other studies, and outside departments.</li><li style=\"color: black; vertical-align: baseline;\">Participate in and cooperate with any internal and external audits or reviews of study protocols; prepare necessary documentation.</li></ul><p style=\"margin-left: 0.5in; vertical-align: baseline;\">&nbsp;</p></td></tr></tbody></table></figure><p>&nbsp;</p></td></tr><tr><td width=\"83\" valign=\"top\" style=\"border: 1pt dotted windowtext; padding: 0in 5.4pt; width: 61.9pt;\"><p style=\"text-align: center;\"><span>100%</span></p></td><td width=\"70\" valign=\"top\" style=\"border-width: medium 1pt 1pt medium; border-style: none dotted dotted none; border-color: currentcolor windowtext windowtext currentcolor; padding: 0in 5.4pt; width: 52.85pt;\">&nbsp;</td><td width=\"546\" valign=\"top\" style=\"border-width: medium 1pt 1pt medium; border-style: none dotted dotted none; border-color: currentcolor windowtext windowtext currentcolor; padding: 0in 5.4pt; width: 409.85pt;\"><i><span style=\"font-size: 9pt;\"><strong>(To update total %, enter the amount of time in whole numbers (without the % symbol - e.g., 15, 20) then highlight the total sum (e.g., 1%) at the bottom of the column and press F9. The total sum should add up to 100%.)</strong></span></i><br><br>&nbsp;</td></tr></tbody></table></figure><p><span><strong>&nbsp;</strong></span>&nbsp;</p><p>&nbsp;</p>",
    "InternalResponsibilitiesStr": "<p style=\"text-align: justify;\">&nbsp;</p><figure class=\"table\"><table border=\"0\" cellspacing=\"0\" cellpadding=\"0\" width=\"699\" style=\"border-collapse: collapse; width: 524.6pt;\"><tbody><tr><td width=\"83\" valign=\"top\" style=\"border: 1pt solid windowtext; padding: 0in 5.4pt; width: 61.9pt;\"><p style=\"text-align: center;\">%&nbsp;</p><p style=\"text-align: center;\"><strong>of time</strong></p></td><td width=\"70\" style=\"border: 1pt solid windowtext; padding: 0in 5.4pt; width: 52.85pt;\"><p style=\"text-align: center;\"><span style=\"font-size: 7pt;\"><strong>Essential Function (Yes/No</strong>)</span></p></td><td width=\"546\" valign=\"top\" style=\"border: 1pt solid windowtext; padding: 0in 5.4pt; width: 409.85pt;\"><p style=\"text-align: center;\"><span style=\"font-size: 9pt;\"><strong>&nbsp;</strong></span>&nbsp;</p><p style=\"text-align: center;\"><span style=\"font-size: 9pt;\"><strong>Key Responsibilities</strong></span></p><p style=\"text-align: center;\"><i><span style=\"font-size: 9pt;\"><strong>(To be completed by Supervisor)</strong></span></i></p></td></tr><tr><td width=\"83\" valign=\"top\" style=\"border-width: medium 1pt 1pt; border-style: none dotted solid; border-color: currentcolor windowtext windowtext; padding: 0in 5.4pt; width: 61.9pt;\"><p style=\"text-align: center;\">50</p></td><td width=\"70\" valign=\"top\" style=\"border-width: medium 1pt 1pt medium; border-style: none dotted dotted none; border-color: currentcolor windowtext windowtext currentcolor; padding: 0in 5.4pt; width: 52.85pt;\">Yes</td><td width=\"546\" valign=\"top\" style=\"border-width: medium 1pt 1pt medium; border-style: none dotted dotted none; border-color: currentcolor windowtext windowtext currentcolor; padding: 0in 5.4pt; width: 409.85pt;\"><figure class=\"table\"><table border=\"0\" cellspacing=\"0\" cellpadding=\"0\" style=\"border-collapse: collapse;\"><tbody><tr><td valign=\"top\" style=\"border: 1pt dotted rgb(170, 170, 170); padding: 0in 5.25pt;\"><h3 style=\"margin: 0in;\"><span style=\"color: black; font-family: Arial, sans-serif;\"><i><span style=\"font-size: 10pt; font-weight: normal;\">Study Coordination and Data Collection</span></i></span></h3><ul style=\"list-style-type: disc;\"><li style=\"color: black; vertical-align: baseline;\">Identify subjects, develop recruitment and retention strategies, and screen and enroll study subjects.</li><li style=\"color: black; vertical-align: baseline;\">Schedule subjects for study visits; meet with them to administer questionnaires, collect medical history<span style=\"font-size: 11pt;\">&nbsp;</span>and perform study procedures.</li><li style=\"color: black; vertical-align: baseline;\">Maintain rapport and relationships with subjects to ensure effective communication and retention; respond to their diverse needs, schedule follow-up appointments, and become their intermediary; discuss study outcomes with providers to ensure continuity of care.</li><li style=\"color: black; vertical-align: baseline;\">Obtain informed consent; review information with subjects; assess and advocate for patient safety throughout each protocol procedure.</li><li style=\"color: black; vertical-align: baseline;\">Oversee subject reimbursement; work to resolve discrepancies and issues.<span>&nbsp; &nbsp; &nbsp; &nbsp; &nbsp;</span></li><li style=\"color: black; vertical-align: baseline;\">Work with staff to ensure procedures are completed, specimens properly stored, and required data collected at visits; and ensure correct shipping and labeling measures.</li><li style=\"color: black; vertical-align: baseline;\">Coordinate, communicate and network with other studies and technicians to ensure scheduling efficiency; communicate with any affiliated groups.</li><li style=\"color: black; vertical-align: baseline;\">Conduct reviews of medical charts and electronic records to extract medical information and other data for use in studies.</li><li style=\"color: black; vertical-align: baseline;\">Implement needs assessments and recommendations for enhancements on patient coordination, data collection, data management, protocol adherence and study collaboration.</li><li style=\"color: black; vertical-align: baseline;\">Attend and actively participate in regular team meetings</li></ul><p style=\"margin-left: 0.5in; vertical-align: baseline;\">&nbsp;</p></td></tr></tbody></table></figure><p>&nbsp;</p></td></tr><tr><td width=\"83\" valign=\"top\" style=\"border-width: medium 1pt 1pt; border-style: none dotted solid; border-color: currentcolor windowtext windowtext; padding: 0in 5.4pt; width: 61.9pt;\"><p style=\"text-align: center;\">20</p><p>&nbsp;</p></td><td width=\"70\" valign=\"top\" style=\"border-width: medium 1pt 1pt medium; border-style: none dotted dotted none; border-color: currentcolor windowtext windowtext currentcolor; padding: 0in 5.4pt; width: 52.85pt;\">Yes</td><td width=\"546\" valign=\"top\" style=\"border-width: medium 1pt 1pt medium; border-style: none dotted dotted none; border-color: currentcolor windowtext windowtext currentcolor; padding: 0in 5.4pt; width: 409.85pt;\"><figure class=\"table\"><table border=\"0\" cellspacing=\"0\" cellpadding=\"0\" style=\"border-collapse: collapse;\"><tbody><tr><td valign=\"top\" style=\"border: 1pt dotted rgb(170, 170, 170); padding: 0in 5.25pt;\"><h3 style=\"margin: 0in;\"><span style=\"color: black; font-family: Arial, sans-serif;\"><i><span style=\"font-size: 10pt; font-weight: normal;\">Data management and reporting of results</span></i></span></h3><ul style=\"list-style-type: disc;\"><li style=\"color: black; vertical-align: baseline;\">Collect data during subject visits; enter data from visits, procedures, lab tests, and other subject-related participation into databases in a timely manner.</li><li style=\"color: black; vertical-align: baseline;\">Manage database structure for each protocol; update databases to improve data analysis and management; create new databases as needed.</li><li style=\"color: black; vertical-align: baseline;\">Create and maintain comprehensive data sets as requested by the CRC Supervisor and/or PI. &nbsp;</li><li style=\"color: black; vertical-align: baseline;\">Maintain data collection forms for effective data collection, entry, and analysis. &nbsp;</li><li style=\"color: black; vertical-align: baseline;\">Perform queries and analysis in databases.</li><li style=\"color: black; vertical-align: baseline;\">Work with Supervisor to maintain complete and accurate data in the study database; analyze the data as they become available.</li></ul><p style=\"margin-left: 0.5in; vertical-align: baseline;\">&nbsp;</p></td></tr></tbody></table></figure><p>&nbsp;</p></td></tr><tr><td width=\"83\" valign=\"top\" style=\"border-width: medium 1pt 1pt; border-style: none dotted solid; border-color: currentcolor windowtext windowtext; padding: 0in 5.4pt; width: 61.9pt;\"><p style=\"text-align: center;\">5</p></td><td width=\"70\" valign=\"top\" style=\"border-width: medium 1pt 1pt medium; border-style: none dotted dotted none; border-color: currentcolor windowtext windowtext currentcolor; padding: 0in 5.4pt; width: 52.85pt;\">&nbsp;</td><td width=\"546\" valign=\"top\" style=\"border-width: medium 1pt 1pt medium; border-style: none dotted dotted none; border-color: currentcolor windowtext windowtext currentcolor; padding: 0in 5.4pt; width: 409.85pt;\"><p><span style=\"color: black;\"><i>Quality control procedures&nbsp;</i></span></p><ul style=\"list-style-type: disc;\"><li style=\"color: black; vertical-align: baseline;\">Oversee data&nbsp;integrity; initiate assessments of the adequacy of existing policies and procedures on subject recruitment, data collection, and data management. &nbsp;</li><li style=\"color: black; vertical-align: baseline;\">Update and maintain a procedure manual documenting all study-related procedures; help develop a plan to ensure consistency in data collection and data entry.</li><li style=\"color: black; vertical-align: baseline;\">Implement and maintain periodic quality control procedures</li><li style=\"color: black; vertical-align: baseline;\">Suggest modifications to the administrative infrastructure to accommodate increasing complexity of studies. &nbsp;</li><li style=\"color: black; vertical-align: baseline;\">Modify data collection instruments</li><li style=\"color: black; vertical-align: baseline;\">Maintain subject tracking systems.</li><li style=\"color: black; vertical-align: baseline;\">Arrange the exchange of and transport of specimens with collaborating Investigators and staff.</li><li style=\"color: black; vertical-align: baseline;\">Some specimen processing such as centrifugation, aliquoting, and shipping may be required in some studies</li><li style=\"color: black; vertical-align: baseline;\">Oversee the incoming data interpreted from samples and ensure that it is utilized correctly for analysis and publications.</li><li style=\"color: black; vertical-align: baseline;\">Ensure integrity and security of samples.</li><li style=\"color: black;\">If the incumbent is a certified phlebotomist, perform phlebotomy as needed.<span>&nbsp;</span></li></ul></td></tr><tr><td width=\"83\" valign=\"top\" style=\"border-width: medium 1pt 1pt; border-style: none dotted solid; border-color: currentcolor windowtext windowtext; padding: 0in 5.4pt; width: 61.9pt;\"><p style=\"text-align: center;\">5</p></td><td width=\"70\" valign=\"top\" style=\"border-width: medium 1pt 1pt medium; border-style: none dotted dotted none; border-color: currentcolor windowtext windowtext currentcolor; padding: 0in 5.4pt; width: 52.85pt;\">&nbsp;</td><td width=\"546\" valign=\"top\" style=\"border-width: medium 1pt 1pt medium; border-style: none dotted dotted none; border-color: currentcolor windowtext windowtext currentcolor; padding: 0in 5.4pt; width: 409.85pt;\"><figure class=\"table\"><table border=\"0\" cellspacing=\"0\" cellpadding=\"0\" style=\"border-collapse: collapse;\"><tbody><tr><td valign=\"top\" style=\"border: 1pt dotted rgb(170, 170, 170); padding: 0in 5.25pt;\"><h3 style=\"margin: 0in;\"><span style=\"color: black; font-family: Arial, sans-serif;\"><i><span style=\"font-size: 10pt; font-weight: normal;\">Study Implementation</span></i></span></h3><p style=\"margin-left: 0.5in; vertical-align: baseline;\">&nbsp;</p></td></tr></tbody></table></figure><p>&nbsp;</p></td></tr><tr><td width=\"83\" valign=\"top\" style=\"border-width: medium 1pt 1pt; border-style: none dotted solid; border-color: currentcolor windowtext windowtext; padding: 0in 5.4pt; width: 61.9pt;\"><p style=\"text-align: center;\">5</p></td><td width=\"70\" valign=\"top\" style=\"border-width: medium 1pt 1pt medium; border-style: none dotted dotted none; border-color: currentcolor windowtext windowtext currentcolor; padding: 0in 5.4pt; width: 52.85pt;\">&nbsp;</td><td width=\"546\" valign=\"top\" style=\"border-width: medium 1pt 1pt medium; border-style: none dotted dotted none; border-color: currentcolor windowtext windowtext currentcolor; padding: 0in 5.4pt; width: 409.85pt;\"><figure class=\"table\"><table border=\"0\" cellspacing=\"0\" cellpadding=\"0\" style=\"border-collapse: collapse;\"><tbody><tr><td valign=\"top\" style=\"border: 1pt dotted rgb(170, 170, 170); padding: 0in 5.25pt;\"><h3 style=\"margin: 0in;\"><span style=\"color: black; font-family: Arial, sans-serif;\"><i><span style=\"font-size: 10pt; font-weight: normal;\">Specimen Management/ Maintenance</span></i></span></h3><p style=\"margin-left: 0.5in; vertical-align: baseline;\">&nbsp;</p></td></tr></tbody></table></figure><p>&nbsp;</p></td></tr><tr><td width=\"83\" valign=\"top\" style=\"border-width: medium 1pt 1pt; border-style: none dotted solid; border-color: currentcolor windowtext windowtext; padding: 0in 5.4pt; width: 61.9pt;\"><p style=\"text-align: center;\">10</p></td><td width=\"70\" valign=\"top\" style=\"border-width: medium 1pt 1pt medium; border-style: none dotted dotted none; border-color: currentcolor windowtext windowtext currentcolor; padding: 0in 5.4pt; width: 52.85pt;\">&nbsp;</td><td width=\"546\" valign=\"top\" style=\"border-width: medium 1pt 1pt medium; border-style: none dotted dotted none; border-color: currentcolor windowtext windowtext currentcolor; padding: 0in 5.4pt; width: 409.85pt;\"><p><span style=\"color: black;\"><i>Protocol Submissions and Adherence</i></span></p><ul style=\"list-style-type: disc;\"><li style=\"color: black; vertical-align: baseline;\">Enter all existing and new study protocols into the Committee on Human Research (CHR) online system; seek assistance on maintaining all protocols in the system by communicating with CHR Analysts.</li><li style=\"color: black; vertical-align: baseline;\">Design and enhance case report forms and data collection forms as needed; provide manuscript feedback; continue to develop and maintain systems for assuring protocol adherence and data quality.</li><li style=\"color: black; vertical-align: baseline;\">Participate in the review and writing of protocols and related procedures to ensure institutional review board approval within University compliance.</li><li style=\"color: black; vertical-align: baseline;\">Renew, modify, and submit CHR applications and protocols; ensure that protocol applications are submitted in a timely manner; serve as a liaison between CHR and study Investigators.</li><li style=\"color: black; vertical-align: baseline;\">Provide quality assurance checks to note if protocols or UCSF CHR applications need to be modified; evaluate protocols on an ongoing basis and implement improvements as needed.</li></ul></td></tr><tr><td width=\"83\" valign=\"top\" style=\"border-width: medium 1pt 1pt; border-style: none dotted solid; border-color: currentcolor windowtext windowtext; padding: 0in 5.4pt; width: 61.9pt;\"><p style=\"text-align: center;\">5</p></td><td width=\"70\" valign=\"top\" style=\"border-width: medium 1pt 1pt medium; border-style: none dotted dotted none; border-color: currentcolor windowtext windowtext currentcolor; padding: 0in 5.4pt; width: 52.85pt;\">&nbsp;</td><td width=\"546\" valign=\"top\" style=\"border-width: medium 1pt 1pt medium; border-style: none dotted dotted none; border-color: currentcolor windowtext windowtext currentcolor; padding: 0in 5.4pt; width: 409.85pt;\"><figure class=\"table\"><table border=\"0\" cellspacing=\"0\" cellpadding=\"0\" style=\"border-collapse: collapse;\"><tbody><tr><td valign=\"top\" style=\"border: 1pt dotted rgb(170, 170, 170); padding: 0in 5.25pt;\"><h3 style=\"margin: 0in;\"><span style=\"color: black; font-family: Arial, sans-serif;\"><i><span style=\"font-size: 10pt; font-weight: normal;\">Regulatory responsibilities</span></i></span></h3><ul style=\"list-style-type: disc;\"><li style=\"color: black; vertical-align: baseline;\">Assure studies are carried out according to Code of Federal Regulations, Good Clinical Practice, and UCSF regulations.</li><li style=\"color: black; vertical-align: baseline;\">Initiate and follow-up on CHR submissions and modifications; track approval status.</li><li style=\"color: black; vertical-align: baseline;\">Interface with departments to obtain UCSF approval prior to study initiation.</li><li style=\"color: black; vertical-align: baseline;\">Maintain regulatory documents; monitor timelines for data submission; document adverse events and submit to appropriate departments.</li><li style=\"color: black; vertical-align: baseline;\">Use sound judgment to maintain patient confidentiality when communicating with agencies, healthcare providers, other studies, and outside departments.</li><li style=\"color: black; vertical-align: baseline;\">Participate in and cooperate with any internal and external audits or reviews of study protocols; prepare necessary documentation.</li></ul><p style=\"margin-left: 0.5in; vertical-align: baseline;\">&nbsp;</p></td></tr></tbody></table></figure><p>&nbsp;</p></td></tr><tr><td width=\"83\" valign=\"top\" style=\"border: 1pt dotted windowtext; padding: 0in 5.4pt; width: 61.9pt;\"><p style=\"text-align: center;\"><span>100%</span></p></td><td width=\"70\" valign=\"top\" style=\"border-width: medium 1pt 1pt medium; border-style: none dotted dotted none; border-color: currentcolor windowtext windowtext currentcolor; padding: 0in 5.4pt; width: 52.85pt;\">&nbsp;</td><td width=\"546\" valign=\"top\" style=\"border-width: medium 1pt 1pt medium; border-style: none dotted dotted none; border-color: currentcolor windowtext windowtext currentcolor; padding: 0in 5.4pt; width: 409.85pt;\"><i><span style=\"font-size: 9pt;\"><strong>(To update total %, enter the amount of time in whole numbers (without the % symbol - e.g., 15, 20) then highlight the total sum (e.g., 1%) at the bottom of the column and press F9. The total sum should add up to 100%.)</strong></span></i><br><br>&nbsp;</td></tr></tbody></table></figure><p><span><strong>&nbsp;</strong></span>&nbsp;</p><p>&nbsp;</p>",
    "InternationalTravelRequired": null
  },
  "list_job": {
    "Id": "2771",
    "Title": "Clinical Research Coordinator Nephrology",
    "JobType": null,
    "Distance": 1780272000000,
    "JobShift": null,
    "Language": "US",
    "WorkDays": null,
    "JobFamily": null,
    "Relevancy": 7,
    "WorkHours": null,
    "Department": null,
    "HotJobFlag": false,
    "PostedDate": "2026-06-01",
    "StudyLevel": null,
    "WorkerType": null,
    "GeographyId": 100000008360352,
    "JobFunction": null,
    "JobSchedule": null,
    "BusinessUnit": null,
    "ContractType": null,
    "ManagerLevel": null,
    "Organization": null,
    "TrendingFlag": true,
    "workLocation": [
      {
        "Country": "US",
        "Region1": "San Francisco",
        "Region2": "CA",
        "Region3": null,
        "Building": null,
        "Latitude": 37.76957,
        "Longitude": -122.44356,
        "LocationId": 300000009343061,
        "PostalCode": "94117",
        "TownOrCity": "San Francisco",
        "AddressLine1": "500 Parnassus Avenue",
        "AddressLine2": "Millberry Union",
        "AddressLine3": "E408",
        "AddressLine4": null,
        "LocationName": "Millberry Union - FL 04 - RM E408"
      }
    ],
    "LegalEmployer": null,
    "MediaThumbURL": null,
    "WorkplaceType": "",
    "BusinessUnitId": 300000007556001,
    "OrganizationId": 300000007556001,
    "PostingEndDate": null,
    "LegalEmployerId": 300000007380777,
    "PrimaryLocation": "San Francisco, CA, United States",
    "WorkDurationYears": null,
    "WorkplaceTypeCode": null,
    "BeFirstToApplyFlag": false,
    "WorkDurationMonths": null,
    "otherWorkLocations": [],
    "secondaryLocations": [],
    "ShortDescriptionStr": "",
    "requisitionFlexFields": [],
    "DomesticTravelRequired": null,
    "PrimaryLocationCountry": "US",
    "ExternalQualificationsStr": null,
    "ExternalResponsibilitiesStr": null,
    "InternationalTravelRequired": null
  },
  "detail_meta": {
    "url": "https://iazuqy.fa.ocs.oraclecloud.com/hcmRestApi/resources/latest/recruitingCEJobRequisitionDetails?expand=all&onlyData=true&finder=ById;Id=%222771%22,siteNumber=CX_1",
    "http_status": 200,
    "content_type": "application/json",
    "response_bytes": 48702
  },
  "detail_errors": []
}
Get this page with API

Rendered from the bluedoor Job Postings API. Reproduce it:

GET https://api.bluedoor.sh/job-postings/v1/jobs/8a3d913b2efeaf4975e4f6d5f08b9b852dfd9c45?include=descriptionJSON
GET https://api.bluedoor.sh/job-postings/v1/orgs/b73f2bf1-b0ab-47ed-8db1-1f14a038aa7cJSON
GET https://api.bluedoor.sh/job-postings/v1/sources/1ec01ec1-9ec0-4ca7-9242-3de42049e519JSON
GET https://api.bluedoor.sh/job-postings/v1/jobs/8a3d913b2efeaf4975e4f6d5f08b9b852dfd9c45/eventsJSON

Docs · Get an API key