Clinical Research Coordinator, Varying Levels

The Rector & Visitors of the University of Virginia; Charlottesville, Virginia, Evanston Township (VA, MN, IL); On-site; USD 50,000 - 80,000; Full time

Job summary

An established industry player is seeking a Clinical Research Coordinator to join their Gynecological Oncology team. This role involves a variety of clinical research duties, including participant recruitment, data collection, and collaboration with research teams. Ideal candidates will possess strong organizational and communication skills, along with a passion for clinical research. This position offers an opportunity to contribute to impactful clinical trials while working in a supportive environment that values teamwork and excellence. If you're eager to make a difference in healthcare, this role could be the perfect fit for you.

Qualifications

• Bachelor's degree required for CRC roles; licensure preferred for some positions.
• 1+ years of clinical research experience preferred for higher levels.

Responsibilities

• Recruit, screen, and enroll study participants for clinical trials.
• Collect, analyze, and report data following research protocols.
• Prepare documentation and maintain logs for participant tracking.

Skills

Organizational Skills

Problem-Solving Abilities

Teamwork Skills

Communication Skills

Assessment Skills

Quick Learner

Education

Bachelor's Degree

Associate's Degree with Licensure

Master's Degree (related)

Job description

Analysis of the Job Description

The job description is comprehensive and detailed, covering responsibilities, qualifications, and application procedures. It uses HTML tags effectively to structure the content, enhancing readability. However, it could be improved by reducing redundancy, correcting minor formatting issues, and ensuring consistency in listing qualifications.

Specifically, some sections are overly verbose, and the formatting of lists could be more uniform. The content remains relevant and focused on the role, with no extraneous information. The minimum requirements are well outlined, matching the responsibilities described.

Refined Job Description

Department of OBGYN - Clinical Research Coordinator (Varying levels)

The Department of OBGYN is seeking a Clinical Research Coordinator (Varying levels) to join our Gynecological Oncology team. The roles include performing clinical research duties such as working with research participants, processing laboratory specimens, data entry, record keeping, and reviewing prospective research participants. Coordinators will assist with clinical trial activities, recruit, screen, and consent participants, schedule visits, maintain documentation, collect data, compile adverse events, and manage all collected data.

Ideal candidates must have strong organizational skills, problem-solving abilities, teamwork skills, excellent communication, assessment skills, and a quick learner.

Key Responsibilities

1. Recruit, screen, and enroll study participants for multiple clinical trials in GynOnc.
2. Obtain informed consent and maintain contact with participants.
3. Collaborate with Principal Investigators and study teams on research projects.
4. Report potential issues with studies or participants.
5. Collect, analyze, and report data following research protocols.
6. Communicate effectively with sponsors.
7. Prepare documentation, reports, graphs, and study materials; keep logs and track participants.
8. Process and ship laboratory specimens.
9. Perform other duties as assigned.

Qualifications

Qualifications vary by level:

• CRC 1, L/NL: Bachelor's degree (non-licensed) or Associate's degree with licensure (licensed).
• CRC 2, L/NL: Bachelor's degree, 1+ year clinical research experience; CCRP/CCCRC preferred, required within one year.
• CRC 3, L/NL: Bachelor's degree, 4+ years experience; related Master's may substitute for 2 years; CCRP/CCCRC preferred, required within one year.
• CRC 4, L/NL: Bachelor's degree, 6+ years experience; related Master's may substitute for 2 years; CCRP/CCCRC preferred, required within one year.

Licensed roles require licensure in a clinical profession (e.g., RN, Pharmacology).

Additional Information

This is a restricted, exempt, benefited position, not supported for VISA. The position is contingent on project needs, funding, and performance. The application remains open until filled. Background checks and health screens are required. Physical demands include extensive computer work, patient interaction, and travel within UVA facilities. Travel to other UVA clinics may be necessary.

Application Process

Please apply online referencing R0054955, including CV, cover letter, and other documents in a single PDF. Internal applicants should apply via their UVA Workday profile. References will be collected via UVA's Skill Survey. For questions, contact Eric Allen at [e-mail].

For more about UVA and Charlottesville, visit http://www.virginia.edu/life/charlottesville and https://embarkcva.com/.

UVA is committed to diversity and equal opportunity employment.