Clinical Research Regulatory Coordinator II
Brigham and Women(5 days ago)
About this role
The Regulatory Affairs Coordinator II at Mass General Brigham supports the management and submission of regulatory documents for clinical trials, ensuring compliance with relevant guidelines. The role involves coordinating with sponsors and IRB committees, maintaining regulatory documentation, and assisting in trial initiation and amendments. It is a remote position based in Boston with a focus on regulatory processes and documentation in clinical research.
Required Skills
- Regulatory Documentation
- IRB Submissions
- Clinical Trials
- GCP Guidelines
- Electronic Systems
- Data Integrity
- Regulatory Compliance
- Documentation Management
- Communication Skills
- Attention to Detail
Qualifications
- Bachelor's Degree in Healthcare Management or Related Field
- 2-3 Years Regulatory Affairs Experience
About Brigham and Women
brighamandwomens.orgBrigham and Women’s Hospital is one of the top hospitals in America with more than 790 beds, and a premier teaching hospital of Harvard Medical School. Learn more.
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