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Sterling Life Sciences, Specialists in Pharmaceuticals, Healthcare and BioTech Recruitment
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 Job #02328 Email this job to a friend
About our client
Our client is a publicly traded pharmaceutical company headquartered in Michigan with over 10 years of success in the development and commercialization of nephrology and urology therapeutics. The company has an experienced management team, a robust pipeline and an empowering corporate culture that is focused on the professional development of its employees.
Position Location
Clinical Project Manager Midwest, USA
Salary
Highly competitive package, commensurate with experience
Responsibilities
1) Manage activities within the Clinical Operations Department relating to the planning/execution of trials
2) Lead in coordinating development of the study protocol
3) Develop drafts of study level/site level budget
4) Negotiate site contracts and budgets
5) Participate in vendor selection teams (CROs, central labs and EDC vendors)
Requirements
1) Bachelor’s degree in a scientific discipline
2) 5+ years of clinical trial experience in the pharmaceutical or biotech industry
3) Nephrology or urology experience (ESRD preferred)
4) 2+ years of clinical project management experience
5) Experience in leading project/study teams
6) Hands-on experience in CRO management, people management and budgets
7) Strong knowledge and understanding of FDA Regulations and GCPs
8) Excellent analytical/problem solving skills
9) Exceptional communication skills

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