Under general direction of Clinical Research Supervisor, the Senior Clinical Research Coordinator has an advance-level working knowledge of data management activities, excellent communication skills and ability to work in a team environment to independently coordinate, direct and ensure follow through for overall administration and outcome of multiple clinical studies. This position will include oversight and training of new or lower-level clinical research coordinators and/or other support personnel, coordinating research meetings and acting as a resource. This 100% position will work with the PIs, other department personnel, sponsors, and community physicians to support and provide guidance on the administration of the regulatory coordination, data management, compliance, patient navigation, personnel and other related aspects of oncology and transplant related clinical studies. This is a grant funded position.
• Certification by the Society of Clinical Research Associates (SoCRA) or the Association of Clinical Research Professionals (ACRP)
• IRB CITI training
• Laboratory Safety Training
• IATA & 49 CFR Certificate
All departmental required certificates and training to obtained within 90 days from date of hire.
• Bachelor’s degree in a science or related ?eld, or an equivalent combination of education and experience.
• Extensive experience in Industry Sponsored clinical trial processes; clinical and regulatory.
• Extensive knowledge of FDA and IRB regulations, ICH guidelines and current Good Clinical Practice (cGCP).
• Experience working with computer systems and databases, including Windows, Microsoft Office Suite, electronic medical records, central trial management system, and electronic data capture systems for clinical research.
• Communication skills to convey factual information; to engage in collaborative problem-solving and negotiation with staff and colleagues.
• Self-directed and able to work independently, meeting the scope of the program with minimal supervision and with frequent changes in priorities and deadlines.
• Ability to independently exercise judgment, initiative and resourcefulness in making decisions.
• Demonstrate oral communication and interpersonal skills to effectively correspond with the general public, co- workers, physicians, patients, caregivers, clinic staff and other health care professionals.
• Display organizational skills and attention to detail so that large volumes of records can be accurately maintained, and workload priorities can be determined in an appropriate way to accomplish a task or goal. Ability to multi-task.
• Ability to work cooperatively as a team in a diverse workforce.
• Three or more years of experience in Phase 1 or oncology clinical trials.
• Advanced-level knowledge of basic anatomy, medical terminology and ability to interpret physicians’ notes, medical records, laboratory and scan results.
• Advanced-level knowledge and understanding of oncology and disease processes as applied to clinical research.
• This position is a critical position and subject to a background check and drug screen. Employment is contingent upon successful completion of background investigation including criminal history, identity checks and drug screen.
• As a condition of employment, you will be required to comply with the University of California Policy on Vaccination Programs, as may be amended or revised from time to time. Federal, state, or local public health directives may impose additional requirements.
To view full job description and submit an on-line application visit UC Davis Career Opportunities at:
Job ID #63402
The University of California, Davis is an Affirmative Action/Equal Opportunity Employer