What are the responsibilities and job description for the Clinical SAS Programmer position at Katalyst Healthcares & Life Sciences?
Responsibilities:
- Conduct high-quality statistical programming including developing and maintaining SAS programs tailored to clinical development programs' needs.
- Generate SDTM domains and Adam datasets.
- Generate tables, figures, and listings as described in statistical analysis plans.
- Provide statistical programming support to exploratory analyses both internally and in response to regulatory agencies' ad-hoc requests.
- Participate in the development of CRFs, edit check specifications, and data validation plans.
- Define and maintain data repository folder contents associated with statistical programming.
- Review SOPs and/or Work Instructions related to statistical programming practices.
- Collaborate with internal and external functions (e.g. CROs, software vendors, clinical development partners, etc) to ensure meeting project timelines and goals.
- Oversee statistical programming contractors.
- BA/BS degree in mathematics, science or health related field.
- Minimum 5 years of programming experience using SAS.
- Base/Stat/Macro/GRAPH in the biopharmaceutical and/or CRO industries; a MS
- Data Management experience and knowledge of CDISC standard are
- Good SAS programming skills and attention to detail are
- Demonstrate knowledge of regulatory biostatistics, SOPs, and Highly motivated and able to work well independently.
- Strong organizational, time management, communication and project coordination and leadership skills.
- Must be able to work well under timeline pressure.
