Home › Companies › Iazuqy Fa Ocs Oraclecloud Com CX 1 › Assistant Clinical Research Coordinator
Assistant Clinical Research Coordinator
Iazuqy Fa Ocs Oraclecloud Com CX 1 · San Francisco, CA, United States; Moffitt Hospital - FL 13 - RM M1329, San Francisco, CA, US · Active · Oracle Recruiting Cloud / Fusion HCM
Job facts
| Field | Value |
|---|---|
| Company | Iazuqy Fa Ocs Oraclecloud Com CX 1 |
| Title | Assistant Clinical Research Coordinator |
| Normalized title | - |
| Department / team | Research and Laboratory |
| Location | San Francisco, CA, United States |
| Work model | - |
| Employment type | Full Time |
| Salary | - |
| Status | active |
| ATS provider | Oracle Recruiting Cloud / Fusion HCM |
| Posted / first seen | 2026-05-30 / 2026-05-31 |
| Changed / last seen | 2026-06-03 / 2026-06-06 |
Related slices
| Page | What it contains | Open |
|---|---|---|
| Company jobs | Active postings from Iazuqy Fa Ocs Oraclecloud Com CX 1. | Open |
| Company breakdowns | Role, location, ATS, and work model facets for this company. | Open |
| ATS provider jobs | Active postings observed through Oracle Recruiting Cloud / Fusion HCM. | Open |
| Provider filtered search | The same provider as a filtered job collection. | Open |
| City jobs | Active postings in San Francisco. | Open |
| Department jobs | Active postings in Research and Laboratory. | Open |
| Lifecycle events | Open, update, close, and reopen events for this posting. | Open |
| Original posting | Canonical source or apply URL captured from the ATS. | Open |
Linked records
| Company | Iazuqy Fa Ocs Oraclecloud Com CX 1 |
| Source | 1ec01ec1-9ec0-4ca7-9242-3de42049e519 |
| ATS provider | Oracle Recruiting Cloud / Fusion HCM |
Description
Description
The UCSF Bronchiectasis and Pulmonary Nontuberculous Mycobacterium (NTM) program comprises clinicians from the Pulmonary and Infectious Disease divisions who collaborate to care for patients with complex pulmonary disease and pulmonary infections. Research, including clinical trials of new therapeutics and prospective observational studies, is a critical part of the program’s mission. The program is seeking an Assistant Clinical Research Coordinator (aCRC) to assist with the daily operations of our research enterprise.
The aCRC will be trained by investigators with the Divisions of Pulmonary Medicine and Infectious Diseases and by an existing network of CRCs and aCRCs within the division. The aCRC will perform entry-level duties related to the execution, management, and coordination of research protocols, as directed by the Principal Investigator (PI) and/or Co-Investigator (co-I). The incumbent will coordinate the data collection and operations of several concurrent clinical research studies under the guidelines of research protocols, UCSF, and regulating agency policies. Activities will be supervised by a senior CRC, PI, and co-PI.
The duties may include, but will not be limited to, supporting the management and coordinating the tasks of single or multiple clinical research studies, depending on their size and complexity; acting as intermediary between services and departments while overseeing data and specimen management; managing and reporting on study results; creating, cleaning, updating, and managing databases and comprehensive reports; managing the Investigators’ protocols in the Committee on Human Research online system and central IRB systems, as well as renewals and modifications of protocol applications and the implementation of new studies, under the supervision of the PI or senior CRC; participating in the review and writing of protocols to ensure institutional review board approval within University compliance; helping assure compliance with all relevant regulatory agencies; overseeing study data integrity; interfacing with departments to obtain UCSF approval prior to study initiation; maintaining all regulatory documents; reporting study progress to investigators; participating in any internal and external audits or reviews of study protocols; resolves operational aspects of clinical studies or trials in conjunction with PI and senior CRC in accordance with standard operating procedures and good clinical practice and regulations; and performing other duties as assigned.
Responsibilities
%
of time (Nothing less than 5%)
Essential Function (Yes/No )
Key Responsibilities
(To be completed by Supervisor)
30
YES
Study Coordination and Data Collection Receive training on how to, and work under CRC and investigators to:
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. Arrange the exchange of and transport of specimens with collaborating Investigators and staff. Oversee the incoming data interpreted from samples and ensure that it is utilized correctly for analysis and publications. 30
YES
Data management and reporting of results
Receive training on how to, and under supervision with a CRC:
Abstract clinical data from medical records (i.e. procedures, lab tests, and other subject-related participation) enter data onto case report forms for The Primary Ciliary Dyskinesia Foundation and the Bronchiectasis Patient Registry in a timely manner.
Develop and maintain Excel spreadsheets
Prepare reports from Apex reports on clinic attendance and health screening
Address and resolve data queries
Identify, investigate and resolve data quality issues
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 Investigators.
Receiving training to manage and maintain RedCap data entry and extraction
Receive training to manage and maintain QuesGen database
Work with Supervisor to maintain complete and accurate data in the study database; analyze the data as they become available.
Help obtain participant biospecimens and receive training to process for storage.
15
YES
Protocol Submissions and Adherence
Receive training on how to, and work under CRC and investigators to:
Enter all existing and new study protocols into the Committee on Human Research (CHR) online system and external IRB systems; seek assistance on maintaining all protocols in the system by communicating with CHR Analysts. 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 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
YES
Quality control and Regulatory responsibilities
Receive training on how to, and work under CRC and investigators to:
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 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. 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. Suggest modifications to accommodate increasing complexity of studies. Modify data collection instruments Maintain subject tracking systems Assess feasibility of new proposed studies 5
YES
Study Implementation
Work under supervision with a CRC to:
10
YES
Biospecimen processing
Receive training on how to, and under supervision with a CRC/PI:
Ensure integrity and security of biospecimens. Collection, transfer, and preliminary processing of biospecimens per laboratory best practices and biosafety regulations. Maintain database structure and linkage of biorepository-clinical repository using best research practices, data integrity standards, and HIPAA compliance.
5
YES
Miscellaneous
Helps prepare for audits/monitoring visits by sponsors and/or regulatory agencies
Attend quarterly meetings with COPD foundation and PCD foundation to receive updated protocols and collaborative conversations of data quality
Help prepare annual reports to COPD Foundation for Care Center grant.
Maintains and updates materials and resources supporting INTEGRATE
Monitors study supply inventory and reorders as needed
Maintains research charts and study binders; and performs other related duties as assigned.
Receive training and under direct supervision p articipate in the renewal, modification, and submission of CHR applications and protocols.
Assist with the quality assurance/modification of protocols or UCSF CHR applications.
10 0%
(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
HS graduation and sufficient experience and demonstrated skills to successfully perform the assigned duties and responsibilities; and/or equivalent experience/training Excellent verbal and written communications and presentation skills ; excellent organizational skills; and excellent interpersonal skills to work effectively in a diverse team. Proficiency with Microsoft Word, PowerPoint, Windows. Excel is required Excellent analytical and problem-solving skills. Ability to work effectively in a fast-paced, team-based environment; project management and coordination skills; ability to prioritize tasks and meet multiple deadlines on concurrent projects. Ability to establish cooperative working relationships with patients, co-workers, & physicians. 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:
Bachelor’s degree in related area and/or equivalent experience/training Demonstrated proficiency with medical terminology. Experience working with patients or study subjects. Ability to abstract data from medical records and transfer it to data collection forms or directly into databases. Experience in RedCap or similar databases Experience with electronic medical records, specifically experience with EPIC Systems Phlebotomy
Full job record
| Job ID | b586c320fe9d247d63a3fac87d253c4e61eaf04e |
| Org ID | b73f2bf1-b0ab-47ed-8db1-1f14a038aa7c |
| Source ID | 1ec01ec1-9ec0-4ca7-9242-3de42049e519 |
| Board ID | 1ec01ec1-9ec0-4ca7-9242-3de42049e519 |
| Provider | oracle_hcm |
| Provider Job Key | 2318 |
| Title | Assistant Clinical Research Coordinator |
| Normalized Title | — |
| Status | active |
| Active | yes |
| Location Text | San Francisco, CA, United States; Moffitt Hospital - FL 13 - RM M1329, San Francisco, CA, US |
| Department | Research and Laboratory |
| Team | — |
| Employment Type | full_time |
| Workplace Type | — |
| Remote Policy | — |
| Country | United States |
| Region | CA |
| City | San Francisco |
| Salary Raw | Description The UCSF Bronchiectasis and Pulmonary Nontuberculous Mycobacterium (NTM) program comprises clinicians from the Pulmonary and Infectious Disease divisions who collaborate to care for patients with complex pulmonary disease and pulmonary infections. Research, including clinical trials of new therapeutics and prospective observational studies, is a critical part of the program’s mission. The program is seeking an Assistant Clinical Research Coordinator (aCRC) to assist with the daily operations of our research enterprise. The aCRC will be trained by investigators with the Divisions of Pulmonary Medicine and Infectious Diseases and by an existing network of CRCs and aCRCs within the division. The aCRC will perform entry-level duties related to the execution, management, and coordination of research protocols, as directed by the Principal Investigator (PI) and/or Co-Investigator (co-I). The incumbent will coordinate the data collection and operations of several concurrent clinical research studies under the guidelines of research protocols, UCSF, and regulating agency policies. Activities will be supervised by a senior CRC, PI, and co-PI. The duties may include, but will not be limited to, supporting the management and coordinating the tasks of single or multiple clinical research studies, depending on their size and complexity; acting as intermediary between services and departments while overseeing data and specimen management; managing and reporting on study results; creating, cleaning, updating, and managing databases and comprehensive reports; managing the Investigators’ protocols in the Committee on Human Research online system and central IRB systems, as well as renewals and modifications of protocol applications and the implementation of new studies, under the supervision of the PI or senior CRC; participating in the review and writing of protocols to ensure institutional review board approval within University compliance; helping assure compliance with all relevant regulatory agencies; overseeing study data integrity; interfacing with departments to obtain UCSF approval prior to study initiation; maintaining all regulatory documents; reporting study progress to investigators; participating in any internal and external audits or reviews of study protocols; resolves operational aspects of clinical studies or trials in conjunction with PI and senior CRC in accordance with standard operating procedures and good clinical practice and regulations; and performing other duties as assigned. Responsibilities % of time (Nothing less than 5%) Essential Function (Yes/No ) Key Responsibilities (To be completed by Supervisor) 30 YES Study Coordination and Data Collection Receive training on how to, and work under CRC and investigators to: 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. Arrange the exchange of and transport of specimens with collaborating Investigators and staff. Oversee the incoming data interpreted from samples and ensure that it is utilized correctly for analysis and publications. 30 YES Data management and reporting of results Receive training on how to, and under supervision with a CRC: Abstract clinical data from medical records (i.e. procedures, lab tests, and other subject-related participation) enter data onto case report forms for The Primary Ciliary Dyskinesia Foundation and the Bronchiectasis Patient Registry in a timely manner. Develop and maintain Excel spreadsheets Prepare reports from Apex reports on clinic attendance and health screening Address and resolve data queries Identify, investigate and resolve data quality issues 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 Investigators. Receiving training to manage and maintain RedCap data entry and extraction Receive training to manage and maintain QuesGen database Work with Supervisor to maintain complete and accurate data in the study database; analyze the data as they become available. Help obtain participant biospecimens and receive training to process for storage. 15 YES Protocol Submissions and Adherence Receive training on how to, and work under CRC and investigators to: Enter all existing and new study protocols into the Committee on Human Research (CHR) online system and external IRB systems; seek assistance on maintaining all protocols in the system by communicating with CHR Analysts. 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 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 YES Quality control and Regulatory responsibilities Receive training on how to, and work under CRC and investigators to: 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 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. 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. Suggest modifications to accommodate increasing complexity of studies. Modify data collection instruments Maintain subject tracking systems Assess feasibility of new proposed studies 5 YES Study Implementation Work under supervision with a CRC to: 10 YES Biospecimen processing Receive training on how to, and under supervision with a CRC/PI: Ensure integrity and security of biospecimens. Collection, transfer, and preliminary processing of biospecimens per laboratory best practices and biosafety regulations. Maintain database structure and linkage of biorepository-clinical repository using best research practices, data integrity standards, and HIPAA compliance. 5 YES Miscellaneous Helps prepare for audits/monitoring visits by sponsors and/or regulatory agencies Attend quarterly meetings with COPD foundation and PCD foundation to receive updated protocols and collaborative conversations of data quality Help prepare annual reports to COPD Foundation for Care Center grant. Maintains and updates materials and resources supporting INTEGRATE Monitors study supply inventory and reorders as needed Maintains research charts and study binders; and performs other related duties as assigned. Receive training and under direct supervision p articipate in the renewal, modification, and submission of CHR applications and protocols. Assist with the quality assurance/modification of protocols or UCSF CHR applications. 10 0% (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 HS graduation and sufficient experience and demonstrated skills to successfully perform the assigned duties and responsibilities; and/or equivalent experience/training Excellent verbal and written communications and presentation skills ; excellent organizational skills; and excellent interpersonal skills to work effectively in a diverse team. Proficiency with Microsoft Word, PowerPoint, Windows. Excel is required Excellent analytical and problem-solving skills. Ability to work effectively in a fast-paced, team-based environment; project management and coordination skills; ability to prioritize tasks and meet multiple deadlines on concurrent projects. Ability to establish cooperative working relationships with patients, co-workers, & physicians. 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: Bachelor’s degree in related area and/or equivalent experience/training Demonstrated proficiency with medical terminology. Experience working with patients or study subjects. Ability to abstract data from medical records and transfer it to data collection forms or directly into databases. Experience in RedCap or similar databases Experience with electronic medical records, specifically experience with EPIC Systems Phlebotomy |
| Salary Min | — |
| Salary Max | — |
| Salary Currency | — |
| Salary Period | day |
| Source URL | https://iazuqy.fa.ocs.oraclecloud.com/hcmUI/CandidateExperience/en/sites/CX_1/job/2318 |
| Apply URL | https://iazuqy.fa.ocs.oraclecloud.com/hcmUI/CandidateExperience/en/sites/CX_1/job/2318 |
| First Seen At | 2026-05-31 17:57:33Z |
| Last Seen At | 2026-06-06 19:36:14Z |
| Last Checked At | 2026-06-06 19:36:14Z |
| Last Changed At | 2026-06-03 11:09:38Z |
| Inactive At | — |
| Source Posted At | 2026-05-30 00:00:00Z |
| Source Updated At | — |
| Raw Payload Uri | s3://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 |
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"ExternalResponsibilitiesStr": "<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: 62.05pt;\"><p style=\"text-align: center;\">% </p><p style=\"text-align: center;\"><strong>of time (Nothing less than 5%)</strong></p></td><td width=\"73\" style=\"border: 1pt solid windowtext; padding: 0in 5.4pt; width: 54.75pt;\"><p style=\"text-align: center;\"><strong>Essential Function (Yes/No</strong>)</p></td><td width=\"544\" valign=\"top\" style=\"border: 1pt solid windowtext; padding: 0in 5.4pt; width: 407.8pt;\"><p style=\"text-align: center;\"><strong> </strong> </p><p style=\"text-align: center;\"><strong>Key Responsibilities</strong></p><p style=\"text-align: center;\"><i><strong>(To be completed by Supervisor)</strong></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: 62.05pt;\"><p style=\"text-align: center;\">30</p></td><td width=\"73\" 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: 54.75pt;\"><p style=\"text-align: center;\">YES</p></td><td width=\"544\" 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: 407.8pt;\"><h3><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><p style=\"text-align: justify;\"><span>Receive training on how to, and work under CRC and investigators to:</span></p><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 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> </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;<strong> </strong><span>communicate with any affiliated groups.</span></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;\">Oversee the incoming data interpreted from samples and ensure that it is utilized correctly for analysis and publications.</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: 62.05pt;\"><p style=\"text-align: center;\">30</p></td><td width=\"73\" 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: 54.75pt;\"><p style=\"text-align: center;\">YES</p></td><td width=\"544\" 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: 407.8pt;\"><p style=\"text-align: justify;\"><i>Data management and reporting of results</i></p><p style=\"text-align: justify;\"> </p><p>Receive training on how to, and under supervision with a CRC:</p><ul style=\"list-style-type: disc;\"><li class=\"ortl-align-justify\"><p style=\"text-align: justify;\">Abstract clinical data from medical records (i.e. procedures, lab tests, and other subject-related participation) enter data onto case report forms for The Primary Ciliary Dyskinesia Foundation and the Bronchiectasis Patient Registry in a timely manner.</p></li><li class=\"ortl-align-justify\"><p style=\"text-align: justify;\">Develop and maintain Excel spreadsheets </p></li><li class=\"ortl-align-justify\"><p style=\"text-align: justify;\">Prepare reports from Apex reports on clinic attendance and health screening </p></li><li class=\"ortl-align-justify\"><p style=\"text-align: justify;\">Address and resolve data queries</p></li><li class=\"ortl-align-justify\"><p style=\"text-align: justify;\">Identify, investigate and resolve data quality issues</p></li><li class=\"ortl-align-justify\"><p style=\"text-align: justify;\">Manage database structure for each protocol; update databases to improve data analysis and management; create new databases as needed.</p></li><li class=\"ortl-align-justify\"><p style=\"text-align: justify;\">Create and maintain comprehensive data sets as requested by the Investigators.</p></li><li class=\"ortl-align-justify\"><p style=\"text-align: justify;\">Receiving training to manage and maintain RedCap data entry and extraction</p></li><li class=\"ortl-align-justify\"><p style=\"text-align: justify;\">Receive training to manage and maintain QuesGen database </p></li><li class=\"ortl-align-justify\"><p style=\"text-align: justify;\">Work with Supervisor to maintain complete and accurate data in the study database; analyze the data as they become available.</p></li><li class=\"ortl-align-justify\"><p style=\"text-align: justify;\">Help obtain participant biospecimens and receive training to process for storage.</p></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: 62.05pt;\"><p style=\"text-align: center;\">15</p></td><td width=\"73\" 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: 54.75pt;\"><p style=\"text-align: center;\">YES</p></td><td width=\"544\" 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: 407.8pt;\"><p><span style=\"color: black;\"><i>Protocol Submissions and Adherence</i></span></p><p><span>Receive training on how to, and work under CRC and investigators to:</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 and external IRB systems; seek assistance on maintaining all protocols in the system by communicating with CHR Analysts.</li><li style=\"color: black; vertical-align: baseline;\">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 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: 62.05pt;\"><p style=\"text-align: center;\">5</p></td><td width=\"73\" 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: 54.75pt;\"><p style=\"text-align: center;\">YES</p></td><td width=\"544\" 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: 407.8pt;\"><p><i>Quality control and Regulatory responsibilities </i></p><p>Receive training on how to, and work under CRC and investigators to:</p><ul style=\"list-style-type: disc;\"><li>Oversee data integrity; initiate assessments of the adequacy of existing policies and procedures on subject recruitment, data collection, and data management. </li><li>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>Implement and maintain periodic quality control procedures</li><li>Assure studies are carried out according to Code of Federal Regulations, Good Clinical Practice, and UCSF regulations.</li><li>Initiate and follow-up on CHR submissions and modifications; track approval status.</li><li>Maintain regulatory documents; monitor timelines for data submission; document adverse events and submit to appropriate departments.</li><li>Use sound judgment to maintain patient confidentiality when communicating with agencies, healthcare providers, other studies, and outside departments.</li><li>Participate in and cooperate with any internal and external audits or reviews of study protocols; prepare necessary documentation.</li><li>Suggest modifications to accommodate increasing complexity of studies. </li><li>Modify data collection instruments</li><li>Maintain subject tracking systems</li><li>Assess feasibility of new proposed studies</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: 62.05pt;\"><p style=\"text-align: center;\">5</p></td><td width=\"73\" 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: 54.75pt;\"><p style=\"text-align: center;\">YES</p></td><td width=\"544\" 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: 407.8pt;\"><p><i>Study Implementation</i></p><p>Work under supervision with a CRC to:</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: 62.05pt;\"><p style=\"text-align: center;\">10</p></td><td width=\"73\" 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: 54.75pt;\"><p style=\"text-align: center;\">YES</p></td><td width=\"544\" 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: 407.8pt;\"><p>Biospecimen processing</p><p>Receive training on how to, and under supervision with a CRC/PI:</p><ul style=\"list-style-type: disc;\"><li><span style=\"color: black;\">Ensure integrity and security of biospecimens.</span></li><li>Collection, transfer, and preliminary processing of biospecimens per laboratory best practices and biosafety regulations.</li><li>Maintain database structure and linkage of biorepository-clinical repository using best research practices, data integrity standards, and HIPAA compliance.</li></ul><p> </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: 62.05pt;\"><p style=\"text-align: center;\">5</p></td><td width=\"73\" 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: 54.75pt;\"><p style=\"text-align: center;\">YES</p></td><td width=\"544\" 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: 407.8pt;\"><p>Miscellaneous</p><p>Helps prepare for audits/monitoring visits by sponsors and/or regulatory agencies</p><p>Attend quarterly meetings with COPD foundation and PCD foundation to receive updated protocols and collaborative conversations of data quality</p><p>Help prepare annual reports to COPD Foundation for Care Center grant.</p><p>Maintains and updates materials and resources supporting INTEGRATE</p><p>Monitors study supply inventory and reorders as needed</p><p>Maintains research charts and study binders; and performs other related duties as assigned.</p><p> </p><p style=\"text-align: justify;\"><span>Receive training and under direct supervision p</span><span style=\"color: black;\">articipate in the renewal, modification, and submission of CHR applications and protocols.</span></p><p> </p><p style=\"text-align: justify;\"><span>Assist with the quality assurance/modification of protocols or UCSF CHR applications. </span></p></td></tr><tr><td width=\"83\" valign=\"top\" style=\"border: 1pt dotted windowtext; padding: 0in 5.4pt; width: 62.05pt;\"><p style=\"text-align: center;\">10<span>0%</span></p></td><td width=\"73\" 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: 54.75pt;\"><p style=\"text-align: center;\"> </p></td><td width=\"544\" 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: 407.8pt;\"><ul style=\"list-style-type: disc;\"><li style=\"color: black; vertical-align: baseline;\"><span style=\"color: windowtext;\"><i><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></i></span></li></ul></td></tr></tbody></table></figure>",
"InternalResponsibilitiesStr": "<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: 62.05pt;\"><p style=\"text-align: center;\">% </p><p style=\"text-align: center;\"><strong>of time (Nothing less than 5%)</strong></p></td><td width=\"73\" style=\"border: 1pt solid windowtext; padding: 0in 5.4pt; width: 54.75pt;\"><p style=\"text-align: center;\"><strong>Essential Function (Yes/No</strong>)</p></td><td width=\"544\" valign=\"top\" style=\"border: 1pt solid windowtext; padding: 0in 5.4pt; width: 407.8pt;\"><p style=\"text-align: center;\"><strong> </strong> </p><p style=\"text-align: center;\"><strong>Key Responsibilities</strong></p><p style=\"text-align: center;\"><i><strong>(To be completed by Supervisor)</strong></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: 62.05pt;\"><p style=\"text-align: center;\">30</p></td><td width=\"73\" 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: 54.75pt;\"><p style=\"text-align: center;\">YES</p></td><td width=\"544\" 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: 407.8pt;\"><h3><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><p style=\"text-align: justify;\"><span>Receive training on how to, and work under CRC and investigators to:</span></p><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 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> </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;<strong> </strong><span>communicate with any affiliated groups.</span></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;\">Oversee the incoming data interpreted from samples and ensure that it is utilized correctly for analysis and publications.</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: 62.05pt;\"><p style=\"text-align: center;\">30</p></td><td width=\"73\" 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: 54.75pt;\"><p style=\"text-align: center;\">YES</p></td><td width=\"544\" 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: 407.8pt;\"><p style=\"text-align: justify;\"><i>Data management and reporting of results</i></p><p style=\"text-align: justify;\"> </p><p>Receive training on how to, and under supervision with a CRC:</p><ul style=\"list-style-type: disc;\"><li class=\"ortl-align-justify\"><p style=\"text-align: justify;\">Abstract clinical data from medical records (i.e. procedures, lab tests, and other subject-related participation) enter data onto case report forms for The Primary Ciliary Dyskinesia Foundation and the Bronchiectasis Patient Registry in a timely manner.</p></li><li class=\"ortl-align-justify\"><p style=\"text-align: justify;\">Develop and maintain Excel spreadsheets </p></li><li class=\"ortl-align-justify\"><p style=\"text-align: justify;\">Prepare reports from Apex reports on clinic attendance and health screening </p></li><li class=\"ortl-align-justify\"><p style=\"text-align: justify;\">Address and resolve data queries</p></li><li class=\"ortl-align-justify\"><p style=\"text-align: justify;\">Identify, investigate and resolve data quality issues</p></li><li class=\"ortl-align-justify\"><p style=\"text-align: justify;\">Manage database structure for each protocol; update databases to improve data analysis and management; create new databases as needed.</p></li><li class=\"ortl-align-justify\"><p style=\"text-align: justify;\">Create and maintain comprehensive data sets as requested by the Investigators.</p></li><li class=\"ortl-align-justify\"><p style=\"text-align: justify;\">Receiving training to manage and maintain RedCap data entry and extraction</p></li><li class=\"ortl-align-justify\"><p style=\"text-align: justify;\">Receive training to manage and maintain QuesGen database </p></li><li class=\"ortl-align-justify\"><p style=\"text-align: justify;\">Work with Supervisor to maintain complete and accurate data in the study database; analyze the data as they become available.</p></li><li class=\"ortl-align-justify\"><p style=\"text-align: justify;\">Help obtain participant biospecimens and receive training to process for storage.</p></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: 62.05pt;\"><p style=\"text-align: center;\">15</p></td><td width=\"73\" 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: 54.75pt;\"><p style=\"text-align: center;\">YES</p></td><td width=\"544\" 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: 407.8pt;\"><p><span style=\"color: black;\"><i>Protocol Submissions and Adherence</i></span></p><p><span>Receive training on how to, and work under CRC and investigators to:</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 and external IRB systems; seek assistance on maintaining all protocols in the system by communicating with CHR Analysts.</li><li style=\"color: black; vertical-align: baseline;\">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 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: 62.05pt;\"><p style=\"text-align: center;\">5</p></td><td width=\"73\" 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: 54.75pt;\"><p style=\"text-align: center;\">YES</p></td><td width=\"544\" 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: 407.8pt;\"><p><i>Quality control and Regulatory responsibilities </i></p><p>Receive training on how to, and work under CRC and investigators to:</p><ul style=\"list-style-type: disc;\"><li>Oversee data integrity; initiate assessments of the adequacy of existing policies and procedures on subject recruitment, data collection, and data management. </li><li>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>Implement and maintain periodic quality control procedures</li><li>Assure studies are carried out according to Code of Federal Regulations, Good Clinical Practice, and UCSF regulations.</li><li>Initiate and follow-up on CHR submissions and modifications; track approval status.</li><li>Maintain regulatory documents; monitor timelines for data submission; document adverse events and submit to appropriate departments.</li><li>Use sound judgment to maintain patient confidentiality when communicating with agencies, healthcare providers, other studies, and outside departments.</li><li>Participate in and cooperate with any internal and external audits or reviews of study protocols; prepare necessary documentation.</li><li>Suggest modifications to accommodate increasing complexity of studies. </li><li>Modify data collection instruments</li><li>Maintain subject tracking systems</li><li>Assess feasibility of new proposed studies</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: 62.05pt;\"><p style=\"text-align: center;\">5</p></td><td width=\"73\" 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: 54.75pt;\"><p style=\"text-align: center;\">YES</p></td><td width=\"544\" 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: 407.8pt;\"><p><i>Study Implementation</i></p><p>Work under supervision with a CRC to:</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: 62.05pt;\"><p style=\"text-align: center;\">10</p></td><td width=\"73\" 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: 54.75pt;\"><p style=\"text-align: center;\">YES</p></td><td width=\"544\" 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: 407.8pt;\"><p>Biospecimen processing</p><p>Receive training on how to, and under supervision with a CRC/PI:</p><ul style=\"list-style-type: disc;\"><li><span style=\"color: black;\">Ensure integrity and security of biospecimens.</span></li><li>Collection, transfer, and preliminary processing of biospecimens per laboratory best practices and biosafety regulations.</li><li>Maintain database structure and linkage of biorepository-clinical repository using best research practices, data integrity standards, and HIPAA compliance.</li></ul><p> </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: 62.05pt;\"><p style=\"text-align: center;\">5</p></td><td width=\"73\" 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: 54.75pt;\"><p style=\"text-align: center;\">YES</p></td><td width=\"544\" 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: 407.8pt;\"><p>Miscellaneous</p><p>Helps prepare for audits/monitoring visits by sponsors and/or regulatory agencies</p><p>Attend quarterly meetings with COPD foundation and PCD foundation to receive updated protocols and collaborative conversations of data quality</p><p>Help prepare annual reports to COPD Foundation for Care Center grant.</p><p>Maintains and updates materials and resources supporting INTEGRATE</p><p>Monitors study supply inventory and reorders as needed</p><p>Maintains research charts and study binders; and performs other related duties as assigned.</p><p> </p><p style=\"text-align: justify;\"><span>Receive training and under direct supervision p</span><span style=\"color: black;\">articipate in the renewal, modification, and submission of CHR applications and protocols.</span></p><p> </p><p style=\"text-align: justify;\"><span>Assist with the quality assurance/modification of protocols or UCSF CHR applications. </span></p></td></tr><tr><td width=\"83\" valign=\"top\" style=\"border: 1pt dotted windowtext; padding: 0in 5.4pt; width: 62.05pt;\"><p style=\"text-align: center;\">10<span>0%</span></p></td><td width=\"73\" 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: 54.75pt;\"><p style=\"text-align: center;\"> </p></td><td width=\"544\" 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: 407.8pt;\"><ul style=\"list-style-type: disc;\"><li style=\"color: black; vertical-align: baseline;\"><span style=\"color: windowtext;\"><i><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></i></span></li></ul></td></tr></tbody></table></figure>",
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