Clinical Trials Regulatory Specialist
Job Summary
To support the advancement of MRI technologies for lymphatic imaging, the full-time Clinical Trials Regulatory Specialist will coordinate regulatory approvals, commercialization plans, and project management tasks, primarily in a remote capacity.
Key responsibilities
- Coordinate the development and implementation of commercialization plans and regulatory roadmaps for new MRI contrast agents
- Manage project timelines, facilitate team meetings, and assist in the organization of presentations and documentation for funding proposals
- Monitor compliance with Institutional Review Board protocols and serve as the lead contact for regulatory agencies
Required qualifications
- Experience with clinical trials, drug development regulation, and commercialization efforts
- Familiarity with Institutional Review Board (IRB) protocols
- Basic knowledge of MRI technology
- Strong organizational skills and the ability to work independently with minimal supervision
- Prior experience collaborating with research teams and study sponsors
Complete Job Description
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