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Sterling Life Sciences, Specialists in Pharmaceuticals, Healthcare and BioTech Recruitment
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 Job #03009 Email this job to a friend
About our client
Our client, a world-leading CRO, provides a broad range of services to the pharmaceutical, biotech and healthcare industries for the development and commercialization of various therapeutics.
Position Location
Associate Director/Project Manager New York/New Jersey/North Carolina
Salary
Highly competitive package, commensurate with experience
Responsibilities
1) Direct, supervise and manage regional/global projects related to Phase II and Phase III clinical trials
2) Manage the scope of work, objectives, quality of deliverables and other activities on large, long-term and complex projects
3) Serve as the primary contact with the client and ensure that appropriate communication channels are maintained
4) Work with Business Services to finalize scope of work and project budget
5) Manage project budgets
6) Supervise maintenance of information and tracking systems
7) Participate in proposal development
Requirements
1) Bachelor's degree in Life Sciences or a related field
2) 10 years of clinical research experience
3) 6 years of project management experience
4) Experience in a key CRO/pharmaceutical operational function (e.g., data management, clinical operations, laboratory, pre-clinical, etc.)
5) Professional Project Management accreditation
6) Excellent communication and interpersonal skills
7) Superb influencing and negotiation skills
8) Good team leadership and customer service skills
9) Excellent decision-making skills and judgment
10) Proficiency in software and computers including MS Office applications
11) Ability to establish and maintain effective working relationships with co-workers, managers and clients
12) Willingness and ability to travel (up to 30%)

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