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Sr / Principal Clinical Programmer San Francisco / Hybrid
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- Founded in 2015, the company has built a portfolio of 20+ drug development programs ranging from preclinical to late-stage development in multiple therapeutic areas including genetic dermatology, precision oncology, cardiology, endocrinology, neurology, pulmonology, and renal disease, with two approved drugs.
- Responsibilities Creates standard and/or custom programs/reports using data analytics tools such as SAS, Tableau, or other data visualization tools to support data oversight and review by data managers or other data reviewers
- Collaborates with Clinical Operations, Data Management, Clinical Development, Drug Safety, Statistical Programming, and Biostatistics to develop standard and custom data reports for quality data oversight / clinical data review
- Generates safety surveillance and/or safety quality data review outputs and patient profiles for Drug Safety and Clinical Development clinical data review
- Provides leadership, training, guidance, and support to other department members on data review tools such as SAS
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