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The Clinical Programming Senior Manager is responsible to manage the timely and accurate execution of programming components of clinical trials.
The Senior Manager leads and manages completed projects, that involved global tasks or cross functional teams or outsourcing resources. The role may require providing inputs to design and analysis, and report the results of clinical trials including programming rules and mocked T/L/G; In addition, providing all safety claims for new drugs and extension of claims/publication support for our marketed drugs.
Essential Duties & Responsibilities:
Education Required: Bachelor's or higher degree in Science, Statistics, Information Technology or equivalent combination of education and related work experience.
Experience Required: 10+ years of professional experience in pharmaceutical or clinical research.
Functional Knowledge: Excellent SAS knowledge of the following SAS modules/ procedures: Base SAS; SAS report writing; SAS macros\ functions.
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