Clinical Trial Coordinator - 12 Months - North NJ - Urgent

Clinical Trial Coordinator - 12 Months - North NJ - Urgent

- Responsible for providing support to the Clinical Study Manager.

Duties include:

- Set up and maintain tracking system for patient visits, contracts, budgets, invoices, vendor and site payments, regulatory documents, IRB approvals, etc.
- Assist Study Manager with electronic study tracking and maintaining a shared electronic study database. Assist Study Manager to create agendas and meeting minutes. Responsible for making routine calls to study sites to request information or to follow-up on action items. Responsible for responding to routine inquiries from internal and external customers to ensure that critical issues are handled appropriately.

Act as a liaison for vendors.

- Strong computer skills required (EXCEL, PowerPoint).

Must have skills:

- Bachelor's degree.
- Min 5 years experience in the management of Clinical Studies in the Pharmaceutical Industry.
- Understanding of ICH, GCP Guidelines required

Rate: $45 an hour
Duration: 12 Months
Location: North New Jersey

Please send me your most up to date CV ASAP if you are interested in this
requirement.
To find out more about Real please visit www.realstaffing.com