Clinical Study Manager

Clinical Study Manager needs 5 years relevant experience is required with a BSc, 3 years with a MS/MPH, or 2 years with PharmD/PhD/MD

Clinical Study Manager requires:

• Phase II/III Oncology trial experience strongly preferred
• Global trial experience strongly preferred
• Experience working in both sponsor and CRO organizations strongly preferred
• Candidates with a nursing diploma/assoc degree with substantial experience may be considered for this position.
• clinical or basic research in a Pharmaceutical company, a Medical device/Diagnostic company, Academic Research Organization (ARO) or
  Contract Research Organization (CRO). CRA experience is preferred. Time spent directly in a medical environment (e.g. as a Study Site
  Coordinator) is also considered relevant.

Clinical Study Manager duties are:

• Develop project cross-functional, integrated study plan to study start up
  (in-house) and validate and manage to the overall study implementation plan provided by the CRO. Participate in site selection and site qualification with (study team and CRO).
• Contribute to operational delivery aspects of the protocol and lead document review
  & coordination for the protocol and amendments.
• Additional medical writing tasks may involve ICF, CRF guidelines, IB and safety communications, DSUR, IND.

$57/hr

6 months