Clinical Contracts Manager
Edison-New Brunswick Metro Area, NJ
Perform and manage all activities associated with the development of clinical site contracts from study concept through to final protocol.
Deliver clinical site agreements that protect business interests and compliance with regulations and laws concerning the same.
2+ years performing clinical contracting and CRO oversight;
3+ years in the Pharmaceutical Industry
BA/BS degree or equivalent (Paralegal or Juris Doctorate is a plus, but not required)
2+ years Clinical Site Contract and Budget negotiation experience
a. Negotiation, analytical, meeting management, cross-functional team and leadership skills required
b. Knowledge of Good Clinical Practice (GCPs) as relates to clinical trial management required
c. Knowledge of contracts workflow systems (e.g. Quickbase) is highly desirable
d. Knowledge in developing/maintaining guidelines, training programs, policies and procedures for the functional area
e. Advanced knowledge of contract terms and conditions (T&C) ***
f. *Advanced knowledge of financial terms, budgets and financial benchmarking ***