Cancer Center Jobs

Regulatory Clinical Research Coordinator

UC Davis Comprehensive Cancer Center

October 29, 2021
Regulatory Clinical Research Coordinator (CRC or Sr.CRC) – SOM: Cancer Center -Sacramento Campus
JO# 19812 

Link to apply

Department Description 

The Office of Clinical Research is dedicated to conducting clinical trials that promote and support multidisciplinary collaborations. These will assist in the translation of our scientific discoveries to the clinic and ultimately bring more lifesaving treatments to our patients. Our mission is to offer our patients the most advanced, personalized therapies that will lead to a reduction in the morbidity and mortality from cancer.

Job Summary 

Final Filing Date                      

11/25/2021

Salary Range                        

 CRC: $29.16 - $46.88

Sr.. CRC: $35.38 - $56.89

Salary Frequency                   

 Hourly

Appointment Type                   

 Career

Number of Positions 

 3

Percentage of Time                 

 100%

Shift Hour                                

 Manager will advise

Location                                   

 Cancer Center

City                                          

Sacramento

Union Representation              

Yes

Benefits Eligible                       

Yes

We offer exceptional employment benefits including medical, dental, and vision plans, generous paid vacations and holidays, excellent retirement savings and investment plans, continuing education, and reduced fee and scholarship programs.  

 THIS IS NOT AN H1- B OPPORTUNITY 

 *Candidate will be hired as CRC or Sr. CRC based on qualifications.

Responsibilities 

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/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.

EEO 

The University of California is an Equal Opportunity/Affirmative Action Employer advancing inclusive excellence.  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 categories covered by the UC nondiscrimination policy.