Job Summary
An information technology company is seeking a Telecommute Clinical Regulatory Device Specialist.
Core Responsibilities of this position include:
- Analyzing clinical data, journal articles and scientific presentations
- Managing one or more post-approval, post-market surveillance clinical trials
- Developing clinical plan strategies and assisting in the execution of clinical study protocols
Skills and Requirements Include:
- 5+ years of experience as a Clinical Research Associate, Clinical Project Manager or equivalent
- Demonstrated clinical regulatory experience
- Knowledge of applicable US and OUS regulations
- Applied knowledge of project management tools
- Demonstrated interpersonal, written and oral communication skills