Clinical Study Manager

Global Channel Management is a technology company specializing in various types of recruiting and staff augmentation. Our account managers and recruiters have over a decade of experience in various verticals. GCM understands the challenges companies face regarding the skills and experience needed to fill the void of day-to-day functions. Organizations need to reduce training and labor costs while requiring the best "talent" for the job.

The Clinical Study Manager position requires:

• 5 years of relevant experience with a BSc,
• 3 years with an MS/MPH, or
• 2 years with Pharm
  
  D/PhD/MD.

Additional requirements include:

• 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/associate degree with substantial experience may be considered.
• Experience in clinical or basic research within pharmaceutical, medical device/diagnostic companies, AROs, or CROs. CRA experience is preferred. Experience as a Study Site Coordinator is also relevant.

• Developing a cross-functional, integrated study plan for study start-up (in-house), and managing the overall study implementation plan provided by the CRO. Participate in site selection and qualification.
• Contributing to operational delivery aspects of the protocol, leading document review, and coordination for protocol amendments.
• Performing additional medical writing tasks such as ICF, CRF guidelines, IB, safety communications, DSUR, and IND.