Lead Clinical Research Associate

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