Regulatory Coordinator for Clinical Trials
Job Summary
Working remotely from a New England state, the full-time Regulatory Coordinator for Clinical Trials will manage protocol submissions, prepare regulatory documents, and ensure compliance for Sarcoma clinical research projects.
Key responsibilities
- Prepares and submits protocol applications, amendments, and informed consent documents for SRC and IRB review
- Maintains and organizes regulatory files for assigned studies in compliance with sponsor requirements
- Tracks and manages new protocol start-up progress, ensuring all activities are completed and benchmarks met
Required qualifications
- Bachelor's degree or 1 year of experience as a Dana-Farber Associate Regulatory Coordinator
- 0-1 years of experience in a medical, scientific research, or technology-oriented environment preferred
- Basic understanding of clinical trial conduct
- Proficiency in Microsoft applications and databases
- Experience with medical terminology
Complete Job Description
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