Job Description

Clinical Research Coordinator III

Location: Richmond, VA

Schedule: Monday – Friday, 8:00 AM – 5:00 PM

Overview:

We’re a growing clinical research organization seeking an experienced and motivated Clinical Research Coordinator III to join our Richmond, VA team full-time. This role is perfect for a detail-oriented professional who thrives in a fast-paced research environment and is passionate about patient care, scientific integrity, and advancing new therapies.

About Us:

We partner with physician practices and research sponsors to expand patient access to clinical trials and bring innovative treatments directly into the community. Our mission is to improve patient outcomes through high-quality research and exceptional operational execution.

What You’ll Do:

• Coordinate all aspects of assigned clinical trials from startup through close-out
• Identify, screen, randomize, and enroll study participants
• Conduct patient visits, obtain informed consent, perform assessments, collect specimens, administer medications, and conduct ECGs
• Maintain accurate source documentation and ensure data integrity
• Prepare and submit regulatory and IRB documentation
• Monitor and report adverse events in accordance with sponsor and regulatory guidelines
• Collaborate closely with investigators, monitors, and cross-functional teams to ensure smooth study operations
• Maintain compliance with GCP, FDA, and IRB regulations while meeting study timelines and site goals

Who You Are:

• Passionate about patient care and advancing clinical research
• Experienced in coordinating all phases of clinical trials
• Detail-oriented, organized, and proactive in managing multiple protocols
• An effective communicator who builds strong relationships with investigators, sponsors, and patients
• Knowledgeable of GCP, FDA, and IRB regulations
• Able to work independently while contributing to a collaborative team

Qualifications:

• Minimum 3 years of clinical research coordination experience
• Strong understanding of clinical trial processes and GCP guidelines
• CCRC certification preferred but not required
• Excellent attention to detail, organizational, and communication skills

What Success Looks Like:

• Ownership of assigned studies and patient relationships
• Clear, proactive communication with leadership and study partners
• Consistent adherence to timelines, data quality standards, and compliance requirements
• Engagement in continuous learning and site technology adoption

Ready to make an impact?

Apply today and help advance groundbreaking therapies in gastroenterology, metabolic disease, urology, vaccines, and more.

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