Clinical Research Coordinator-Varying Levels(Licensed)-Cancer Center
About The Position
Looking to make a meaningful impact every day? The Office of Clinical Research (OCR) at the University of Virginia Comprehensive Cancer Center is looking for Clinical Research Coordinators, Licensed (multiple levels) to support the advancement of innovative cancer research. In this role, you will combine your clinical nursing expertise with research coordination to help bring new cancer therapies from study to standard of care by coordinating oncology clinical trials and working closely with patients, physicians, and multidisciplinary research teams. You’ll play a key part in ensuring studies are conducted efficiently, ethically, and in full compliance with regulatory and institutional standards. This is an excellent opportunity for detail-oriented, collaborative professionals who are passionate about high-quality research and motivated to contribute to work that improves and extends patients’ lives.
Requirements
- Strong organizational skills and attention to detail
- A problem-solver mindset and comfort juggling multiple priorities
- Clear, compassionate communication (written and verbal)
- The ability to learn quickly and adapt in a fast-paced research environment
- A collaborative, team-first approach to your work
- Bachelor's Degree Required or equivalent combination of experience, education and or certifications. Nursing Diploma may substitute for Degree for Licensed Registered Nurse.
- Licensed to Practice in Clinical Profession such as (but not limited to): Registered Nurse, Athletic Training, Pharmacology, Medical Technology, Physical Therapy or Registered Respiratory Therapy.
- At least one year of clinical research experience (Clinical Research Coordinator- 2, Licensed)
- A minimum of 3 years of clinical research experience required. Master’s or advanced degree may substitute for 1 year of clinical research experience. (Clinical Research Coordinator- 3, Licensed)
- At least seven years of clinical research experience demonstrating progressive levels of responsibility and complexity of work. Master’s or other advanced degree may substitute for one year of clinical research experience. (Clinical Research Coordinator- 4, Licensed)
- Clinical Research Coordinator (CCRC) and/or Certified Clinical Research Professional (CCRP) is required. (Clinical Research Coordinator- 4, Licensed)
Responsibilities
- Recruit, screen, consent, and enroll participants across multiple cancer clinical trials
- Build trusted relationships with study participants through phone and in-person interactions
- Coordinate study visits and collect high-quality data at each visit
- Maintain accurate documentation, logs, and study materials
- Process, prepare, and ship laboratory specimens
- Track adverse events and ensure protocol compliance
- Collaborate closely with investigators and the research team to keep studies on track
- Integrate nursing skills into clinical research activities
Benefits
- Make a real impact in cancer research and patient care
- Join a mission-driven team at a top academic medical center
- Grow your clinical research career with support and mentorship
- Work in a role that blends science, organization, and meaningful human connection
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What This Job Offers
Job Type
Full-time
Career Level
Entry Level
Number of Employees
1-10 employees
