Job Summary
A drug development company is filling a position for a Remote Clinical Site Activation and Regulatory Affairs Lead.
Must be able to:
- Serve as the primary point of accountability and contact for all start-up activities
- Coordinate and drive the activities of the Site Activation
- Oversee the activities of assigned Regulatory Affairs Specialists
Must meet the following requirements for consideration:
- 4 year college curriculum or 2 year college curriculum or equivalent education/training
- 8 years’ experience within clinical research
- 3+ years CRO/pharmaceutical industry experience
- Project Management, and/or Site Management experience
- Proficient in cross-cultural communication
