Clinical Research Coordinator / Senior Clinical Research Coordinator -SOM: Cancer Center Department- Sacramento Campus

University of California - Davis

United States, California, Sacramento

2000 Stockton Boulevard (Show on map)

July 07, 2023

The UC Davis Comprehensive Cancer Center (UCDCCC) is a matrix organization under the aegis of UC Davis Health and University of California, Davis. Designated by the National Cancer Institute as a Comprehensive Cancer Center, the Center is a clinical and research enterprise consisting of 249 faculty members from the Davis, Sacramento and Lawrence Livermore National Laboratory campuses with research funding totaling $48M.

Job Summary

Final Filing Date	7/21/2023
Salary Range	CRC $30.03 - $48.29 Sr CRC $36.44 - $58.60
Salary Frequency	Hourly
Appointment Type	Career
Number of Positions	1
Percentage of Time	100%
Shift Hour	8 hours
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

Responsibilities

The Clinical Research Coordinator is a health professional having working knowledge of clinical research activities, communication skills and a willingness to cooperate as a team member. Required is the use of skills to independently or with general direction coordinate and follow through in the overall administration and outcome of clinical studies.

The Senior Clinical Research Coordinator is a health professional having an advanced-level working knowledge of data management activities, excellent communication skills and a willingness to cooperate as a team member. The position requires certification by the Society of Clinical Research Associates or the Association of Clinical Research Professionals. Also required is the use of advanced-level knowledge and skills to independently coordinate, direct and follow through in the overall administration and outcome of one or more clinical studies. This position will provide leadership for a department-wide clinic.

Required Qualifications

CRC*

Knowledge and understanding of disease processes as applied to human clinical research.

Knowledge of clinical research trials regulation (Food and Drug Administration [FDA], Office for Human Research Protections [OHRP], and Good Clinical Practice [GCP]).

Knowledge of regulatory processes as well as working knowledge of data management activities as applied to clinical coordination.

Working knowledge of Microsoft office Suite:Word, Excel, Outlook, Access, etc.

Sr. CRC*

Must possess certification by the Society of Clinical Research Associates (SoCRA) or the Association of Clinical Research Professionals (ACRP).

Experience coordinating clinical trials.

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 regulatory processes as well as a working knowledge of data management activities as applied to oncology clinical trial coordination.

Advanced-level experience with oncology disease processes as applied to clinical research.

Advanced-level experience with basic anatomy, medical terminology and ability to interpret physicians' notes, medical records, laboratory and scan results.

Demonstrated leadership skills or experience encompassing both training and ongoing coaching.

Experience with databases and/or Clinical Trial Management System (CTMS).

Preferred Qualifications

Previous experience coordinating oncology clinical trials.

Applicants will be hired at CRC or Sr. CRC level depending on qualifications met.

Bachelor's degree, preferably in the sciences or health related field. Ideal candidate will have at least 2 years relevant experience in the health sciences field and a minimum of 2 years of clinical trials experience

Special Requirements

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 covering all employees. To be compliant with the policy, employees must submit proof of vaccination or a University-approved exception or deferral.

Diversity, Equity, Inclusion and Belonging

At UC Davis, we're solving life's most urgent challenges to bring a fuller, healthier, and more resilient world within reach. We grow from every challenge we take on and we don't just maintain - we improve.

We recognize that creating an inclusive and intellectually vibrant organization means understanding and valuing both our individual differences and our common ground. The most comprehensive solutions come from the most diverse minds and you belong here.

As you consider joining UC Davis, please explore our , our and for research and education, and our latest efforts to .

The 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.