Clinical Research Coordinator: Start-to-Close Trials

Medix

Hampton (VA)

On-site

USD 34,000 - 44,000

Full time

4 days ago

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Job summary

Medix is seeking a detail-oriented Clinical Research Coordinator in Hampton, Virginia to support trials from start-up through closeout. You will coordinate study activities under supervision, ensure compliance with GCP/ICH/IRB, and work closely with investigators, sponsors, CROs, and study teams.

The role requires organizing and balancing patient care with regulatory duties, with responsibilities spanning patient recruitment, data management, and protocol adherence in a fast-paced clinical

Qualifications

Bachelor’s degree with 1+ year of relevant life sciences experience; OR
Associate’s degree with 2+ years of relevant life sciences experience; OR
High school diploma with 3+ years of relevant life sciences experience.

Responsibilities

Coordinate study trials from start-up to closeout.
Screen and prescreen potential participants.
Recruit and enroll eligible patients.
Schedule visits and communicate with participants.
Conduct trial visits per protocol.
Maintain source documentation.
Enter data into sponsor/CRO EDC systems and resolve queries.
Collect regulatory documents for sponsors/IRBs.
Support protocol training and amendments.
Document adverse events and deviations.

Skills

Documentation

Data entry

Patient interaction

Regulatory compliance

Team collaboration

Education

Bachelor's degree

Associate's degree

High school diploma

Tools

EMR/EHR systems

Microsoft Office

Job description

The role requires organizing and balancing patient care with regulatory duties, with responsibilities spanning patient recruitment, data management, and protocol adherence in a fast-paced clinical

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