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Clinical Research Coordinator Surgery

Iazuqy Fa Ocs Oraclecloud Com CX 1 · San Francisco, CA, United States; Daniel Burnham Court - FL 02 - RM 203, San Francisco, CA, US · Active · Oracle Recruiting Cloud / Fusion HCM

Job facts

FieldValue
CompanyIazuqy Fa Ocs Oraclecloud Com CX 1
TitleClinical Research Coordinator Surgery
Normalized title-
Department / teamResearch and Laboratory
LocationSan Francisco, CA, United States
Work model-
Employment type-
Salary-
Statusactive
ATS providerOracle Recruiting Cloud / Fusion HCM
Posted / first seen2026-03-27 / 2026-05-31
Changed / last seen2026-05-31 / 2026-06-22

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PageWhat it containsOpen
Company jobsActive postings from Iazuqy Fa Ocs Oraclecloud Com CX 1.Open
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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
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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 will work independently or under general direction by the Clinical Research Supervisor and/or Principal Investigator (PI) to manage and coordinate research protocols within the Department of Surgery Clinical Research Core. The coordinator will be assigned studies across the 7 divisions in the department based on Principal Investigator needs; may coordinate the data collection and operations of several concurrent clinical research studies under the guidelines of research protocols, UCSF and regulating agency policies. 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 and accuracy; strong interpersonal skills; excellent, effective verbal and written communication skills to coordinate with patients, team members, other departments, outside institutions, and companies. Ability to multitask in a fast-paced environment while working with a diverse population and competing deadlines.Ability to work well independently and in a team setting, take initiative, complete projects in a timely manner, and prioritize multiple responsibilities to ensure the completion of essential tasks by deadlines. Preferred Qualifications BA/BS with biology or public health coursework included.Knowledge of medical terminology.Experience with electronic medical records.Experience with research tools such as REDCap and Qualtrics.Prior analytical and writing skills in a science/research environment.Understanding of patient population to create rapport and a relationship, while giving insight into what is realistic and appropriate for patient participation.Fluency in the usage of the Institutional Review Board (IRB) online systems for the submission, renewal, and modification of research protocols.Certification by the Society of Clinical Research Associates or the Association of Clinical Research Professionals.  Knowledge of UCSF and departmental policies for dealing with research payments and reimbursements;  patient safety and confidentiality; packing/shipping infectious substances; database building/analysis, and data management within some of the following platforms: Access, Stata, SASS/ SPSS, and Teleform.Experience applying the following regulations and guidelines:The Protection of Human Research SubjectsGood Clinical PracticeHealth Insurance Portability and Accountability Act (HIPAA)IRB regulationsSafe shipping practices (IATA)Environmental Health and Safety TrainingFire Safety Training.

Full job record

Job IDbde4e439f4d4069ab88644f2c165fc072a9972f3
Org IDb73f2bf1-b0ab-47ed-8db1-1f14a038aa7c
Source ID1ec01ec1-9ec0-4ca7-9242-3de42049e519
Board ID1ec01ec1-9ec0-4ca7-9242-3de42049e519
Provideroracle_hcm
Provider Job KeyCONV_88341BR
TitleClinical Research Coordinator Surgery
Normalized Title—
Statusactive
Activeyes
Location TextSan Francisco, CA, United States; Daniel Burnham Court - FL 02 - RM 203, San Francisco, CA, US
DepartmentResearch and Laboratory
Team—
Employment Type—
Workplace Type—
Remote Policy—
CountryUnited States
RegionCA
CitySan Francisco
Salary RawDescription The Clinical Research Coordinator will work independently or under general direction by the Clinical Research Supervisor and/or Principal Investigator (PI) to manage and coordinate research protocols within the Department of Surgery Clinical Research Core. The coordinator will be assigned studies across the 7 divisions in the department based on Principal Investigator needs; may coordinate the data collection and operations of several concurrent clinical research studies under the guidelines of research protocols, UCSF and regulating agency policies. 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 and accuracy; strong interpersonal skills; excellent, effective verbal and written communication skills to coordinate with patients, team members, other departments, outside institutions, and companies. Ability to multitask in a fast-paced environment while working with a diverse population and competing deadlines.Ability to work well independently and in a team setting, take initiative, complete projects in a timely manner, and prioritize multiple responsibilities to ensure the completion of essential tasks by deadlines. Preferred Qualifications BA/BS with biology or public health coursework included.Knowledge of medical terminology.Experience with electronic medical records.Experience with research tools such as REDCap and Qualtrics.Prior analytical and writing skills in a science/research environment.Understanding of patient population to create rapport and a relationship, while giving insight into what is realistic and appropriate for patient participation.Fluency in the usage of the Institutional Review Board (IRB) online systems for the submission, renewal, and modification of research protocols.Certification by the Society of Clinical Research Associates or the Association of Clinical Research Professionals.  Knowledge of UCSF and departmental policies for dealing with research payments and reimbursements;  patient safety and confidentiality; packing/shipping infectious substances; database building/analysis, and data management within some of the following platforms: Access, Stata, SASS/ SPSS, and Teleform.Experience applying the following regulations and guidelines:The Protection of Human Research SubjectsGood Clinical PracticeHealth Insurance Portability and Accountability Act (HIPAA)IRB regulationsSafe shipping practices (IATA)Environmental Health and Safety TrainingFire Safety Training.
Salary Min—
Salary Max—
Salary Currency—
Salary Period—
Source URLhttps://iazuqy.fa.ocs.oraclecloud.com/hcmUI/CandidateExperience/en/sites/CX_1/job/CONV_88341BR
Apply URLhttps://iazuqy.fa.ocs.oraclecloud.com/hcmUI/CandidateExperience/en/sites/CX_1/job/CONV_88341BR
First Seen At2026-05-31 17:57:33Z
Last Seen At2026-06-22 15:09:32Z
Last Checked At2026-06-22 15:09:32Z
Last Changed At2026-05-31 17:57:33Z
Inactive At—
Source Posted At2026-03-27 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=2026-06-22/2026-06-22T15-08-04-565Z-700e501ca0122fdf818744e06a8be022bd3d408a345110fe8c8401c4bdb6aaac.json
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