ZipRecruiter

Log In

1

Ucsf Clinical Research Jobs (NOW HIRING)

next page

Showing results 1-20

All JobsUcsf Clinical Research Jobs

UCSF Clinical Research information

See salary details

$49K

$107.3K

$189K

How much do ucsf clinical research jobs pay per year?

As of Jun 12, 2026, the average yearly pay for ucsf clinical research in the United States is $107,336.00, according to ZipRecruiter salary data. Most workers in this role earn between $81,000.00 and $122,500.00 per year, depending on experience, location, and employer.

What are the key skills and qualifications needed to thrive in the Ucsf Clinical Research position, and why are they important?

To thrive in a UCSF Clinical Research role, you need a strong background in clinical research methods, data analysis, and regulatory compliance, usually supported by a relevant degree in health sciences or a related field. Familiarity with tools such as REDCap, electronic data capture systems, and certifications like CITI or Good Clinical Practice is highly valued. Exceptional organizational skills, attention to detail, and the ability to communicate effectively with multidisciplinary teams are crucial soft skills. These competencies ensure accurate study conduct, ethical compliance, and successful collaboration for advancing medical research.

What is a UCSF Clinical Research job?

A UCSF Clinical Research job involves conducting, managing, or supporting medical studies at the University of California, San Francisco. These roles vary from clinical research coordinators to principal investigators, focusing on patient care, data collection, regulatory compliance, and study execution. Employees work closely with scientists, healthcare professionals, and participants to advance medical knowledge and improve treatments.

What are some of the typical day-to-day responsibilities in a UCSF Clinical Research position?

A typical day in a UCSF Clinical Research role may involve recruiting study participants, coordinating study visits, collecting and entering data, and ensuring all regulatory requirements are met. You will often interact with physicians, study coordinators, and other researchers to ensure studies progress smoothly. Additionally, responsibilities can include preparing research documentation, monitoring study protocols for compliance, and contributing to team meetings or study updates. This dynamic work environment encourages collaboration and offers exposure to innovative clinical studies and leading healthcare professionals.

More about UCSF Clinical Research jobs
What cities are hiring for Ucsf Clinical Research jobs? Cities with the most Ucsf Clinical Research job openings:
What are the most commonly searched types of Ucsf Clinical Research jobs? The most popular types of Ucsf Clinical Research jobs are:
What job categories do people searching Ucsf Clinical Research jobs look for? The top searched job categories for Ucsf Clinical Research jobs are:
UCSF Clinical Research jobs near you
Infographic showing various Ucsf Clinical Research job openings in the United States as of June 2026, with employment types broken down into 100% Full Time. Highlights an 100% In-person job distribution, with an average salary of $107,336 per year, or $51.6 per hour.
Clinical Research Supervisor

Clinical Research Supervisor

University of California San Francisco

San Francisco, CA • On-site

Full-time

Posted 26 days ago

Job description

Job Description
Job Summary :The position of Advanced Lung Disease Clinical Research Supervisor is responsible for the overall operational management of the UCSF Advanced Lung Disease Program's clinical research activities. Both of these programs are growing substantially and have significant management responsibilities. This position is critically important to the management of the increased clinical research activities.
The position of Advanced Lung Disease Clinical Research Supervisor involves direct responsibility for implementing a diverse portfolio of research activities including multicenter clinical trials (both NIH and industry-sponsored), local investigator-initiated clinical trials, and programmatic clinical research activities such as the clinical database, and biorepository. The Clinical Research Supervisor is a critical position that requires expert and efficient integration of multiple complex programmatic activities. The position requires substantial leadership skills, the ability to effectively work with multiple different people and organizations at UCSF (clinicians, investigators, clinical staff, administration, committee on human research, human resources, contracts and grants) and elsewhere (industry sponsors, coordinating centers, FDA, NIH), and an in depth knowledge of all aspects of the advanced lung disease programs.
Under the direction of the Director, ILD Program and the Director of Clinical Trials, ILD Program, the Clinical Research Supervisor will have central responsibility for ensuring CHR approval and compliance, contract generation, negotiation and approval, subject recruitment, appropriate study testing, and adequate enrollment of all multicenter clinical trials, longitudinal cohort studies, local investigator-initiated studies, and biorepository efforts. The Advanced Lung Disease Programs need strong administrative and management leadership, strong research coordination, and experienced personnel who can ensure optimal efficiency, compliance, safety, employee supervision and management, financial oversight, and contractual expertise. This position is a position of leadership whose main purpose is to ensure that the programs' clinical research commitments are met and that the program maintains excellence in all its activities.
Qualifications
Required Qualifications :
  • Bachelor's degree in related and five or more years of related experience which includes three or more years of supervisory experience and / or an equivalent combination of education and experience.
  • At least 3 years experience in clinical trial management or equivalent years progressively responsible experience in a related position including regulatory and compliance responsibilities.
  • Three to 5 years in a Lead or Supervisory role.
  • Clinical Trial Professional certification from a professional society within one year in position.
  • Experience serving as a project manager and the ability to develop project plans and schedules and to motivate team members to complete objectives within deadlines.
  • Demonstrated experience in audit preparation, execution, and follow-up.
  • Experience using database software, such as MS Access or Filemaker Pro.
  • Experience with UCSF grant application procedures, personnel documentation and contracts generation, and CARE and UCSF subcontracting.
  • 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 recruitment goals as needed.
  • In-depth and extensive knowledge of clinical research contracts and grants, clinical trials, protocols, FDA regulations, and complex visit structures.
  • Project management skills in order to oversee the administrative operations of the clinical trials program. Specifically, s/he must have knowledge of strategies for recruiting human subjects to research studies as well as skills for HR management and financial analysis
  • Demonstrated skills in preparing and presenting financial and quantitative analyses, including financial projections and budgets.
  • Demonstrated skills in preparing and presenting financial and quantitative analyses, including financial projections and budgets.
  • Fluency in spreadsheet software and the ability to develop independently complex spreadsheets
  • A well-rounded knowledge of human resource management.
  • Previous experience in risk management regarding complicated study subjects, and federal and non-federal sponsors and regulating bodies.
  • 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 interpret and apply policies and regulations.

Preferred Qualifications :
  • Master's degree related scientific/medical area.
  • Certified Clinical Research Coordinator

License / Certification :Yes
License/Certification :
  • Clinical Trial Professional certification from a professional society within one year in position.

Apply