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Job description
Lead statistical programming activities for multiple and/or complex late-stage clinical trial development programs. Act as a key collaborator with biostatisticians, project leads, data managers, and other stakeholders in ensuring that project plans are executed efficiently with timely and high-quality deliverables.
Develop and execute statistical analysis and reporting deliverables, develop SAS and R programs, maintain macro libraries, and coordinate activities of a global programming team.
Must have a strong background in statistical analysis, programming, and project management, with experience in leading large and/or complex statistical programming projects for Phase 2 and 3 clinical trials.
Company
Healthcare
Merck & Co., Inc. (MSD) is a global biopharmaceutical company dedicated to leveraging cutting-edge science to develop innovative medicines and vaccines for both humans and animals. With more than 130 years of research heritage, MSD focuses on advancing prevention and treatment across a broad spectrum of diseases, positioning itself at the forefront of scientific discovery. The company distinguishes itself through a research-intensive culture, a diverse and inclusive workforce, and a commitment to responsible operations that promote sustainable health outcomes worldwide. MSD’s integrated approach to science and stewardship underscores its mission to improve lives and foster a healthier future for all communities.
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