Job Board

The Senior Regulatory Clinical Research Coordinator provides leadership for a department-wide clinical research program, including mentoring and overseeing junior regulatory coordinators and/or other support personnel and possess advanced knowledge of regulatory processes as well as a working knowledge of data management activities. Additionally, the Senior Regulatory Clinical Research Coordinator requires certification by the Society of Clinical Research Associates or the Association of Clinical Research Professionals and is required to have advanced-level knowledge of federal, local, and institutional regulatory guidelines.

The Regulatory Clinical Research Coordinator is a health professional possessing analytical and communication skills, knowledge of FDA/GCP/NIH guidelines, knowledge of IRB policies and procedures, knowledge of data management activities and a willingness to cooperate as a team member.  The Regulatory Coordinator performs duties related to the support and regulatory coordination of clinical studies. Occasional travel and overtime may be required.  

Required Qualifications 

Applicants are encouraged to upload license and certification if required of the position. 

*Sr. CRC

• Certification by the Society of Clinical Research Associates (SoCRA) or the Association of Clinical Research Professionals (ACRP).
• Experience with disease processes as applied to human clinical research.
• Minimum 3 years of clinical trial coordination experience.
• Advanced experience with federal, local, and institutional regulations and policies (e.g., Food and Drug Administration [FDA], Office for Human Research Protections [OHRP], and Good Clinical Practice [GCP]).
• Advanced experience with IRB policies and procedures.
• Advanced experience with anatomy and medical terminology.
• Experience with training and coaching others.
• Experience with Microsoft Office Suite: Word, Excel, Outlook and Access.
• Experience with databases and/or Clinical Trial Management System and (CTMS).
• Experience maintaining large volumes of records.
• Experience composing reports and correspondence while utilizing correct grammar, spelling and punctuation as well as clearly documenting research data onto forms.

*CRC

• Knowledge and understanding of disease processes as applied to human clinical research.
• Knowledge of clinical research trials regulations (e.g., Food and Drug Administration [FDA] and Office for Human Research Protections [OHRP]).
• Knowledge of IRB policies and procedures.
• Knowledge of basic anatomy and medical terminology
• Working knowledge with Microsoft Office Suite: Word, Excel, Outlook, Access, etc.

Preferred Qualifications

Sr. CRC and CRC

• Experience coordinating oncology clinical trials
• Knowledge and understanding of oncology and disease processes as applied to clinical research. 

Special Requirements 

• Must be able to work occasional overtime as work demands.
• Must be able to travel on occasion.?
• This position may be subject to a criminal background investigation, drug screen, Live Scan fingerprinting, medical evaluation clearance, and functional capacity assessment.
• This position may be subject to a criminal background investigation, drug screen, Live Scan fingerprinting, medical evaluation clearance, and functional capacity assessment.
• The University of California has implemented a SARS-CoV-2 (COVID-19) Vaccination Program SARS-CoV-2 Vaccination Policy (ucop.edu) covering all employees.  To be compliant with the policy, employees must submit proof of vaccination or a University-approved exception or deferral.

To view full job description and submit an on-line application visit UC Davis Career Opportunities at:

http://50.73.55.13/counter.php?id=211715

Job ID #19812

The University of California, Davis is an Affirmative Action/Equal Opportunity Employer