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Sterling Life Sciences, Specialists in Pharmaceuticals, Healthcare and BioTech Recruitment
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 Job #03099 Email this job to a friend
About our client
Our client is a world leading CRO. The company provides a broad range of services to the pharmaceutical, biotech and healthcare industries for the development and commercialization of various therapeutics.
Position Location
Clinical Project Manager Louisiana
Salary
Highly competitive package, commensurate with experience
Responsibilities
1) Manage single and full-service clinical projects (both regional and global in scope)
2) Lead cross-functional project teams
3) Ensure quality, on-time and within budget deliverables for Phase I – IV clinical trials
4) Manage the clinical study timelines deliverables and risks
5) Work with the client and business services to finalize the project budget as well as scope
6) Manage clinical projects in overseas locations
7) Participate in internal and external meetings
8) Manage project budgets
9) Serve as the primary contact with the client to ensure appropriate communication
Requirements
1) MS in Life Sciences or a related field (Ph. D. preferred)
2) 10 – 15 years of clinical research or related experience
3) 7+ years of experience in clinical project management
4) Experience in a key CRO/pharmaceutical operational function (e.g. data management, clinical operations, laboratory and pre-clinical)
5) Experience in oncology, neurology, diabetes, cardiology
6) Phase I – IV management experience preferred
7) Knowledge of clinical study guidelines (FDA, ICH and GCP)
8) In-depth understanding of the clinical trials process
9) Willingness to travel to Asian countries (up to 50%)

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