What are the responsibilities and job description for the Principal SAS Programmer position at Princeton Pharmatech?
Princeton Pharmatech is a specialized provider of biostatistics and programming solutions to the pharmaceutical, biotechnology, life science industries, and research institutions worldwide. With headquarters in Princeton, New Jersey and San Francisco, CA, we have provided biostatistics and programming solutions in various therapeutic areas leading to IND and NDA submissions in the US, Europe, and Japan. The Principal SAS Programmer will be responsible for statistical programming for the client’s clinical studies. In this role, you will develop and validate SAS programs for data presentation, analyses, and provide programming support to project team members. Our ideal candidate will have a strong work ethic capable of thriving in a high growth, fast-paced, and intellectual environment.
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Responsibilities
- Serves as lead programmer for assigned projects to provide statistical and programming support in one or more Phase I-III clinical studies.
- Design and perform quality checks on analysis datasets, tables, listings, figures (TFL), and written reports to support clinical trial results using SAS.
- Create and review annotated CRF to STDM datasets.
- Produce and maintain technical programming specification documents.
- Lead and actively participate in client and project review meetings.
- Communicate with clients regarding study protocol or statistical analysis issues.
- Validate statistical deliverables and ensure that appropriate statistical methods are utilized.
- Ensure adherence to industry standards and regulatory requirements.
- Facilitate the development and application of adequate statistical methods in clinical research.
Requirements
Job Category : Principal Statistical Programmer
Job Type : Remote
Job Location : New Jersey
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