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- Clinical trial/study management experience
- Working knowledge of Good Clinical Practices (GCP), monitoring, clinical and regulatory operations
- Experience with CRO oversight
- Demonstrated experience in managing per subject costs, vendor and ancillary, and monitoring costs projections and spend
- Understands feasibility of protocol implementation
- Understands how to work with vendors to accomplish tasksEducation:
- Bachelor's of Science degree or Nurse – minimum of 2 years of relevant experience
- Master's of Science degree or Doctor of Philosophy degree – minimum of 1 year of relevant experience
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Study Manager - Southeast, United States - Parexel
Description
The Study Manager (SM) has responsibility for all study management aspects of assigned studies of limited complexity (e.g., single country, small number of countries) or manage a unique part of a larger study (e.g., recruitment and retention) and manages the tactical execution from study startup through database release and inspection readiness to ensure timely delivery of quality study data.
Knowledge and Experience: