Minimum of 4 years’ experience in Global Clinical Trials.

May perform all or some of the following responsibilities:

1)     May ensure the successful negotiation and ongoing management of clinical trial agreements with investigative sites and vendor agreements and associated budget management.

2)     Maintain accurate records metrics and reports; identify gaps and report to management; make recommendations for process improvement and efficiencies.

3)     May have some accountability for processes or groups of trials; operates with limited oversight.

4)     Achieve successful delivery of site start-up, submission, in-house site management and closeout activities meeting internal and external client requirements.

5)     Responsible for end to end process within country.