Description
Roles and Responsibilities:- Initiate, maintain and reconcile Trial Master File
- Set up and maintain tracking systems and tools and report study metrics to support the clinical study
- Coordinate communication of tracking information within Study Team and to sites
- Coordinate investigator meeting planning in concert with travel planners, including preparing meeting materials and on-site meeting implementation
- Develop study related documents in collaboration with the study team
Requirements:
- 2+ years industry experience in equivalent role
- Bachelors degree or equivalent undergraduate degree
- Working knowledge of international regulatory and ICH GCP guidelines
Other: In-house (South San Francisco), 40 hours/week, minimal (if any) travel required.
To find out more about Real please visit www.realstaffing.com