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Job #03004

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 Clinical Project Manager East Coast/Research Triangle Salary Highly competitive package, commensurate with experience Responsibilities 1) Manage single and full service clinical projects (both regional and global in scope) 2) Lead the cross functional project teams including Clinical Operations, Data Management, Biostatistics, Medical Writing and Clinical QA, to ensure quality, on-time and within budget deliverables for Phase II – IV clinical trials 3) Manage clinical study timelines deliverables and risks 4) Work with the client and business services to finalize the project budget and scope 5) Serve as the primary contact with the client to ensure appropriate communication 6) Manage project budget 7) Participate in internal and external meetings Requirements 1) BS in Life Sciences or a related field 2) 5+ years of clinical research or related experience 3) 2+ years of experience in a project management environment 4) Experience in a key CRO/pharmaceutical operational function (e.g., data management, clinical operations, laboratory and pre-clinical) 5) Experience in oncology 6) Phase II – IV management experience preferred 7) Experience in resource and budget/financial management 8) Knowledge of clinical study guidelines (FDA, ICH and GCP) 9) In-depth understanding of the clinical trials process 10) Excellent communication skills (written and oral) 11) Good client management skills 12) Proficiency in computers/technology (MS Excel, PowerPoint and MS Project as well as similar project management tools)