Licensed Clinical Research Coordinator — Cancer Trials Lead

Virginia AG

Charlottesville (VA)

Hybrid

USD 52,000 - 78,000

Full time

14 days+
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Job summary

The University of Virginia Comprehensive Cancer Center is seeking Licensed Clinical Research Coordinators (CRC) to support oncology trials, combining nursing expertise with research coordination to move therapies from study to standard care.

You will work with patients, physicians, and multidisciplinary teams to ensure studies are conducted ethically, efficiently, and in full compliance with regulatory standards, while growing your clinical research career in a mission-driven academic medical

Qualifications

  • Licensure in clinical profession such as RN, Athletic Training, Pharmacology, Medical Technology, Physical Therapy, or Respiratory Therapy.
  • CRC levels 1–4 with nursing degree substitution rules.
  • Bachelor's Degree required or equivalent; Nursing Diploma may substitute for RN degree.
  • CRC 2 requires at least 1 year of clinical research experience.
  • CRC 3 requires at least 3 years of clinical research experience; advanced degree may substitute.
  • CRC 4 requires at least 7 years of clinical research experience; advanced degree may substitute.

Responsibilities

  • Recruit, screen, consent, and enroll participants across multiple cancer trials.
  • Build trusted relationships with study participants via 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 with investigators to keep studies on track.
  • Integrate nursing skills into clinical research activities.

Skills

Organization
Problem-solving
Communication
Learning agility
Team collaboration

Education

Bachelor's degree

Job description

The University of Virginia Comprehensive Cancer Center is seeking Licensed Clinical Research Coordinators (CRC) to support oncology trials, combining nursing expertise with research coordination to move therapies from study to standard care.

You will work with patients, physicians, and multidisciplinary teams to ensure studies are conducted ethically, efficiently, and in full compliance with regulatory standards, while growing your clinical research career in a mission-driven academic medical

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