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 Job #02627 Email this job to a friend
About our client
Our client is a global organization dealing in pharmaceutical services and deep scientific knowledge with broad execution expertise across the lifecycle continuum. The company concentrates on generating real-world data to support the development and commercialization of medical products for emerging and established life science companies. It specializes in providing new/innovative ways for drug- and devices-related studies.
Position Location
Clinical Project Manager Philadelphia, Pennsylvania
Salary Reports to
Highly competitive package, commensurate with experienceManagement
Responsibilities
1) Anticipate and resolve project needs
2) Ensure that the Case Report Forms (CRFs) meet project needs
3) Assist the protocol development process
4) Coordinate investigator meetings
5) Prepare project timelines
6) Locate appropriate investigators
7) Negotiate budgets/clinical study agreements
8) Prepare appropriate documents for the IRB and the FDA (as necessary)
9) Ensure that all final and interim reports required by the sponsor are completed
10) Act as the primary contact with the sponsor
11) Handle study budgets
12) Develop and maintain Study Master File (SMF)
13) Perform other assigned tasks
Requirements
1) Bachelor's degree in Life Sciences
2) Experience in CNS or oncology a plus
3) 2+ years of experience as a Project Manager
4) Minimum 5 years of clinical research experience, which includes field monitoring
5) Management experience in a CRO environment
6) Experience in project budgeting, Study Master File setup and maintenance, protocol development and bid defense
7) Exceptional communication and presentation skills

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