Top 15 Senior clinical research coordinator Jobs in San Leandro, Ca

Senior Clinical Research Coordinator, Liver Biorepository
University of California San Francisco —San Francisco, CA
- Full-time
- Microsoft Access
- Analysis skills
- Presentation skills
Senior Clinical Research Coordinator Cardiology
University of California San Francisco —San Francisco, CA
- Full-time
- Microsoft Access
- Bachelor of Science
- Analysis skills
Senior Clinical Research Coordinator
University of California San Francisco —San Francisco, CA
- Bachelor of Science
- Analysis skills
- University
Senior Clinical Research Associate
Protagonist Therapeutics —Newark, CA
- $135,000 - $150,000 a year
- English
- Office
- Bachelor's degree
Quick Apply
Senior Scientist, Clinical Research
Merck —San Francisco, CA
- $117,000 - $184,200 a year
- Full-time
- Master's degree
- Bachelor's degree
- Doctor of Philosophy
- Paid holidays
- Health insurance
Senior Clinical Research Associate
Natera —San Carlos, CA
- $99,400 - $124,200 a year
- Bachelor of Science
- HIPAA
- Analysis skills
- Commuter assistance
- Health insurance
Senior Project Manager Clinical Research
Abbott Laboratories —Alameda, CA
- $100,000 - $200,000 a year
- Full-time
- Master's degree
- 8 years
- Travel
- Health insurance
- Tuition reimbursement
Sr. Clinical Research Coordinator - Breast Oncology Program
University of California San Francisco —San Francisco, CA
- Full-time
- Microsoft Access
- Analysis skills
- Presentation skills
15h
Senior Clinical Research Associate (level dependent on experience)
CTI Clinical Trial Services, Inc —San Francisco, CA
- Hybrid work
- Nursing
- Mid-level
- Master's degree
- Paid parental leave
- Tuition reimbursement
Quick Apply
Senior Director, Clinical Research-Oncology
Vir Biotechnology —San Francisco, CA
- $235,500 - $329,500 a year
- Full-time
- Medicine
- 11+ years
- Office
- Commuter assistance
- Paid holidays
Quick Apply
Senior Director, Clinical Research-Infectious Disease
Vir Biotechnology —San Francisco, CA
- $235,500 - $329,500 a year
- Full-time
- Medicine
- Office
- 8 years
- Commuter assistance
- Paid holidays
Quick Apply
Senior Director, Clinical Research-Medical Director (Oncology)
Vir Biotechnology —San Francisco, CA
- $235,500 - $329,500 a year
- Full-time
- Medicine
- BC/BE
- Office
- Commuter assistance
- Paid holidays
Quick Apply
14d
LVN Clinical Coordinator - Home Health
Sequoia Home Health —Milpitas, CA
- $80,000 - $90,000 a year
- Full-time
- LVN
- Mid-level
- 3 years
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9d

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Senior Clinical Research Coordinator, Liver Biorepository

University of California San Francisco -
San Francisco, CA

Apply Now

Job Details

Full-time

Qualifications

Financial forecasting
Contract management
Data analysis reporting
Clinical trial risk management
Team leadership
Budget reports
Data management
Project management experience in healthcare
Financial data management
Contracts
Healthcare team management
Audit risk assessments
Healthcare financial management
Patient recruitment
Financial forecasting analysis
Clinical program risk management
Research and development project management
Organizational budget management
Audit support

Full Job Description

The Senior Clinical Research Coordinator independently coordinates and is accountable for the overall operation of the Ibrahim El-Hefni Liver Biorepository (IELB) and its associated clinical research studies at UCSF. Requiring advanced-level knowledge and skills, the incumbent serves as the operational and regulatory lead for the biorepository—overseeing biospecimen collection, processing, annotation, and distribution—and provides leadership to other clinical research coordinators and support personnel within the program.

This position is critically important to the operational management of the IELB and the liver disease research it supports. It has direct responsibility for managing a biospecimen repository—including blood, serum, plasma, and liver tissue linked to richly annotated clinical data—along with the longitudinal cohort studies and investigator-initiated protocols that feed it. The incumbent prepares and maintains IRB (CHR) applications and approvals, coordinates studies, and actively publicizes the biorepository’s available samples to investigators at UCSF and externally to maximize their scientific use. The role requires expert integration of regulatory, operational, and data-management activities, applying a sophisticated medical and immunology knowledge base and substantial leadership skills, and working effectively with clinicians, investigators, clinical staff, the Committee on Human Research, and contracts and grants staff at UCSF, as well as with external collaborators, sponsors, and NIH.

Reporting to the Principal Investigator/Director, the incumbent has central responsibility for ensuring IRB approval and ongoing compliance for the biorepository and its protocols; managing consent, specimen accessioning, inventory, and chain-of-custody; coordinating biospecimen requests and material transfers; and building and maintaining the IELB website to communicate available samples, governance policies, and request procedures to the research community. The incumbent also leads experienced personnel and implements quality improvement processes. This is a position of leadership whose main purpose is to ensure that the biorepository’s scientific, regulatory, and operational commitments are met and that the program maintains a reputation for excellence in all activities.

The Ibrahim El-Hefni Liver Biorepository (IELB) at UCSF is a translational research resource within the Department of Medicine dedicated to advancing the study of liver disease.. The IELB collects, processes, annotates, and stores high-quality biospecimens—including blood, serum, plasma, and liver tissue and makes these samples available to investigators across UCSF and the broader scientific community. By pairing rigorous regulatory and quality oversight with active outreach to the research community, the IELB accelerates discovery in liver biology and the development of curative therapies. We are a collaborative, mission-driven team seeking an experienced Senior Clinical Research Coordinator to lead the operational, regulatory, and biorepository activities of the program.

Required Qualifications:

Bachelor’s degree in related area and sufficient experience and demonstrated skills to successfully perform the assigned duties and responsibilities and/or equivalent experience/training.
Demonstrated ability to develop recruitment strategies in complex environments and differing patient pools, independently identifying recruitment leads, implementing new strategies, and continually adjusting strategies to meet current recruitment goals.
In-depth knowledge of clinical research contracts and grants, clinical trials, protocols
Project management skills to oversee the administrative operations of the clinical trials program; knowledge of strategies for recruiting human subjects.
Exceptional analytical skills to evaluate the importance and urgency of problems; excellent demonstrated interpersonal, verbal and written communication skills.
Ability to analyze complex and non-routine issues requiring innovative solutions.
Ability to operate effectively in a changing organizational and technological environment.
Ability to assess and respond to audit risk; ability to develop project plans/schedules and motivate team to meet deadlines.
Ability to interpret and apply policies and regulations.
Financial analysis skills; demonstrated skills in preparing and presenting financial and quantitative analyses, including financial projections and budgets.
Significant project and clinical trial management experience or progressively responsible experience in a related position including regulatory and compliance responsibilities.

Required Licenses and/or Certifications:

Ability to obtain certification by the Society of Clinical Research Associates or the Association of Clinical Research Professionals within one year of date of hire.

Preferred Qualifications:

Fluency in spreadsheet software; ability to develop complex spreadsheets independently; demonstrated skills in audit preparation, execution, and follow-up.
Experience in risk management regarding study subjects, federal and non-federal sponsors and regulating bodies.
Experience with grant application procedures, personnel documentation, contract generation and subcontracting, preferably at UCSF.
Certification by the Society of Clinical Research Associates or the Association of Clinical Research Professionals

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

Apply Now

Refine Your Search

senior clinical research coordinator jobs in san leandro, ca

Senior Clinical Research Coordinator, Liver Biorepository

Senior Clinical Research Coordinator Cardiology

Senior Clinical Research Coordinator

Senior Clinical Research Associate

Senior Scientist, Clinical Research

Senior Clinical Research Associate

Senior Project Manager Clinical Research

Sr. Clinical Research Coordinator - Breast Oncology Program

Senior Clinical Research Associate (level dependent on experience)

Senior Director, Clinical Research-Oncology

Senior Director, Clinical Research-Infectious Disease

Senior Director, Clinical Research-Medical Director (Oncology)

LVN Clinical Coordinator - Home Health

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