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Clinical Research Coordinator

Iazuqy Fa Ocs Oraclecloud Com CX 1 · San Francisco, CA, United States; UCSF Pride Hall - FL 04 - RM 4700, San Francisco, CA, US · Active · Oracle Recruiting Cloud / Fusion HCM

Job facts

FieldValue
CompanyIazuqy Fa Ocs Oraclecloud Com CX 1
TitleClinical Research Coordinator
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 seen2026-06-17 / 2026-06-18
Changed / last seen2026-06-21 / 2026-06-21

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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 join a mission-driven research team dedicated to improving care for people with opioid use disorder (OUD) through innovative, patient-centered clinical research. This position provides an exciting opportunity to help launch and coordinate a pragmatic randomized controlled trial (RCT) comparing two approaches to buprenorphine initiation among people using fentanyl. The study is based at the San Francisco Outpatient Buprenorphine Induction Clinic (OBIC) and is a collaboration between UCSF, the San Francisco Department of Public Health, and community partners. The CRC will be part of a close-knit group committed to advancing health equity and expanding access to effective addiction treatment. Working under the direction of the Principal Investigator (PI) and research team, the Clinical Research Coordinator will perform independently or with general direction at the fully operational journey level of the series to execute, manage, and coordinate study protocols. Responsibilities will include coordinating recruitment and enrollment, obtaining informed consent, managing study visits, collecting survey and clinical data, maintaining regulatory compliance, and ensuring smooth day-to-day study operations in accordance with UCSF and federal guidelines. Responsibilities Key Responsibilities Coordinate and manage participant recruitment, screening, enrollment, and follow-up for the randomized controlled trial. Conduct study visits, administer questionnaires and symptom diaries, and collect biological or clinical data as needed. Maintain study databases and manage data entry, cleaning, and quality control procedures. Ensure compliance with study protocols, institutional review board (IRB) requirements, and all UCSF and regulatory agency policies. Assist with study randomization and documentation of study arm allocation (e.g., Low-Dose vs. Direct-to-Inject buprenorphine). Track participant progress and retention and implement procedures to minimize loss to follow-up. Support the development and maintenance of study materials, standard operating procedures (SOPs), and participant tracking systems. Coordinate communication between the research team, clinical staff, and community partners to ensure successful trial implementation. Prepare IRB submissions, protocol amendments, and annual reports; maintain regulatory binders and correspondence. Assist with data analysis, preparation of reports, abstracts, and manuscripts. Participate in regular study meetings, training sessions, and collaborative activities with community and research partners. Qualifications Required Qualifications: College graduation and sufficient experience and demonstrated skills to successfully perform the assigned duties and responsibilities; and/or equivalent experience/training. Prior experience with clinical research: recruiting, interviewing, eliciting informed consent, and explaining study requirements to participants in clinical research studies. Demonstrated communication in and English–written, verbal and interpersonal skills. Excellent verbal and written communications and presentation skills; excellent organizational skills; and excellent interpersonal skills to work effectively in a diverse team. Proficiency with iPhone, Zoom, Microsoft Word, PowerPoint, and Windows. 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 other scientists and community organizations. Demonstrated strong administrative and organizational skills. Prior experience in a healthcare and/or clinical research environment sufficient to understand medical records, confidentiality, and common healthcare information procedures. Preferred Qualifications: Prior experience in conducting and facilitating randomized clinical trials Demonstrated communication in English and Spanish–written, verbal and interpersonal skills. Familiarity with working with populations affected by substance use or structural vulnerabilities. Knowledge of REDCap, Qualtrics, or similar research data management systems. Experience conducting participant interviews or survey administration. Excellent organizational, communication, and interpersonal skills. Ability to work both independently and collaboratively within a diverse, multidisciplinary team. 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 ID47b1cfef28ab125f14393290266a59f0482a1cc0
Org IDb73f2bf1-b0ab-47ed-8db1-1f14a038aa7c
Source ID1ec01ec1-9ec0-4ca7-9242-3de42049e519
Board ID1ec01ec1-9ec0-4ca7-9242-3de42049e519
Provideroracle_hcm
Provider Job Key3452
TitleClinical Research Coordinator
Normalized Title
Statusactive
Activeyes
Location TextSan Francisco, CA, United States; UCSF Pride Hall - FL 04 - RM 4700, San Francisco, CA, US
DepartmentResearch and Laboratory
Team
Employment Typefull_time
Workplace Type
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CountryUnited States
RegionCA
CitySan Francisco
Salary RawDescription The Clinical Research Coordinator (CRC) will join a mission-driven research team dedicated to improving care for people with opioid use disorder (OUD) through innovative, patient-centered clinical research. This position provides an exciting opportunity to help launch and coordinate a pragmatic randomized controlled trial (RCT) comparing two approaches to buprenorphine initiation among people using fentanyl. The study is based at the San Francisco Outpatient Buprenorphine Induction Clinic (OBIC) and is a collaboration between UCSF, the San Francisco Department of Public Health, and community partners. The CRC will be part of a close-knit group committed to advancing health equity and expanding access to effective addiction treatment. Working under the direction of the Principal Investigator (PI) and research team, the Clinical Research Coordinator will perform independently or with general direction at the fully operational journey level of the series to execute, manage, and coordinate study protocols. Responsibilities will include coordinating recruitment and enrollment, obtaining informed consent, managing study visits, collecting survey and clinical data, maintaining regulatory compliance, and ensuring smooth day-to-day study operations in accordance with UCSF and federal guidelines. Responsibilities Key Responsibilities Coordinate and manage participant recruitment, screening, enrollment, and follow-up for the randomized controlled trial. Conduct study visits, administer questionnaires and symptom diaries, and collect biological or clinical data as needed. Maintain study databases and manage data entry, cleaning, and quality control procedures. Ensure compliance with study protocols, institutional review board (IRB) requirements, and all UCSF and regulatory agency policies. Assist with study randomization and documentation of study arm allocation (e.g., Low-Dose vs. Direct-to-Inject buprenorphine). Track participant progress and retention and implement procedures to minimize loss to follow-up. Support the development and maintenance of study materials, standard operating procedures (SOPs), and participant tracking systems. Coordinate communication between the research team, clinical staff, and community partners to ensure successful trial implementation. Prepare IRB submissions, protocol amendments, and annual reports; maintain regulatory binders and correspondence. Assist with data analysis, preparation of reports, abstracts, and manuscripts. Participate in regular study meetings, training sessions, and collaborative activities with community and research partners. Qualifications Required Qualifications: College graduation and sufficient experience and demonstrated skills to successfully perform the assigned duties and responsibilities; and/or equivalent experience/training. Prior experience with clinical research: recruiting, interviewing, eliciting informed consent, and explaining study requirements to participants in clinical research studies. Demonstrated communication in and English–written, verbal and interpersonal skills. Excellent verbal and written communications and presentation skills; excellent organizational skills; and excellent interpersonal skills to work effectively in a diverse team. Proficiency with iPhone, Zoom, Microsoft Word, PowerPoint, and Windows. 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 other scientists and community organizations. Demonstrated strong administrative and organizational skills. Prior experience in a healthcare and/or clinical research environment sufficient to understand medical records, confidentiality, and common healthcare information procedures. Preferred Qualifications: Prior experience in conducting and facilitating randomized clinical trials Demonstrated communication in English and Spanish–written, verbal and interpersonal skills. Familiarity with working with populations affected by substance use or structural vulnerabilities. Knowledge of REDCap, Qualtrics, or similar research data management systems. Experience conducting participant interviews or survey administration. Excellent organizational, communication, and interpersonal skills. Ability to work both independently and collaboratively within a diverse, multidisciplinary team. 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
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Source URLhttps://iazuqy.fa.ocs.oraclecloud.com/hcmUI/CandidateExperience/en/sites/CX_1/job/3452
Apply URLhttps://iazuqy.fa.ocs.oraclecloud.com/hcmUI/CandidateExperience/en/sites/CX_1/job/3452
First Seen At2026-06-18 11:14:49Z
Last Seen At2026-06-21 11:58:17Z
Last Checked At2026-06-21 11:58:17Z
Last Changed At2026-06-21 11:58:17Z
Inactive At
Source Posted At2026-06-17 00:00:00Z
Source Updated At
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