Clinical Trial Coordinator - Regulatory
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Job Summary
Working remotely on a full-time basis, the Clinical Trial Coordinator - Regulatory will manage site contacts, monitor site performance, and assist with regulatory submissions to ensure compliance with study guidelines.
Key responsibilities
- Serve as the primary contact for project teams and investigative sites, documenting all site interactions as required
- Monitor site performance and implement corrective action plans in collaboration with Clinical Research Associates (CRAs)
- Assist in the preparation for site visits and manage the distribution of clinical trial supplies
Required qualifications
- University/College degree in life sciences or certification in a related allied health profession
- At least 1-2 years of clinical research experience
- Basic understanding of biology and biological processes
- Ability to monitor study sites according to protocol and regulatory guidelines
- Good organizational and time management skills
Complete Job Description
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