Responsibilities:
• A statistical programmer consultant provides timely support to the study team on all programming matters according to the project strategies.
• Requirements will be identified according to a Statistical Analysis Plan and programming specifications using internal standards and guidelines. The incumbent implements and executes the programming and project standards.
• Works independently in the design and testing of program logic, coding programs, program documentation and preparation of programs. Supports ongoing clinical studies requests for statistical and non-statistical analyses.
• Meets statistical ad hoc requests of senior management.
• Provides documentation and consistent maintenance of code, logs, and output in a regulated environment.
• Known for its scientific and operational excellence, Regeneron is a leading science-based biopharmaceutical company that discovers, invents, develops, manufactures, and commercializes medicines for the treatment of serious medical conditions.
• Regeneron commercializes medicines for eye diseases, high LDL-cholesterol, atopic dermatitis and a rare inflammatory condition and has product candidates in development in other areas of high unmet medical need, including rheumatoid arthritis, asthma, pain, cancer and infectious diseases.
Requirements:
• Support programmer within a study team involved in the creation and QC of analysis datasets TFL's or standard tools following Regeneron standard data models or user requirements.
• Apply standard tools developed for the study or project. Participate in development of new standards and tools.
• Follow all company SOP and guidelines in the creation of the programming deliverables.
• Adheres to procedures surrounding retention of data, records, and information for clinical studies.
• Experience and Required Skills: Requirements:
• SAS, (Base, Stat, Macro, graph).
• MS. (BS) in Statistics, Computer Science, Mathematics, Engineering, Life Science or related discipline with 5 -7 years of programming experience preferably in processing clinical trial data in the biotechnology, pharmaceutical or health related industry. SAS Certification a plus.
• Experience in SAS programming, preferably in a clinical data environment.
• Exposure of relational database structure
• Understanding of reporting systems.
• Experience with implementing standardization methodology.
• Demonstrated teamwork and interpersonal skills, strong verbal and written communication skills in a global environment.
• Ability to support study requirements with challenging timelines under direct supervision by the programming lead.
Location: New York, NY
Posted: Oct. 4, 2024, 8:44 p.m.
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