Lead Clinical Research Associate
Raritan, NJ, us, United States Contract
Lead Clinical Research Associate needs:
- BS/BA, MS is desirable
- 5+ years of site management of which a minimum of 2 years field monitoring experience
- Knowledge of applicable standards and regulations for clinical trial
- Experience in Cardiovascular Therapeutic area
- IVD Stud Experience
- Medidata RAVE system
Lead Clinical Research Associate duties:
- Under
supervision of Clinical Project Lead, oversees performance of assigned
field monitors and site activities in accordance with the Monitoring
Plan, Protocol, Good Clinical Practice (GCP), ICH guidelines and federal
regulations. - The LCRA acts as a primary liaison between Field
Based CRAs and the Clinical Project Lead (CPL). Additional
responsibilities include: - Implementation of enrollment and recruitment strategies
- Assistance in vendors’ selection processes •
$45/hr
12 months