PROMETRIKA is a full-service clinical research organization (CRO) with extensive experience in clinical operations, data management, biostatistics, medical writing, and pharmacovigilance. We’re driven by our passion for the human aspect of our work and our compassion for the people whose lives have been improved by the innovations we help bring to market. Our clients include national and international biopharmaceutical and medical device companies of all sizes.
RESPONSIBILITIES:
- Under guidance of a statistical programmer or biostatistician, develop SAS programs to produce simple tables and listings (TLs) for individual study reports in accordance with table/listing shells
- Assist in the creation of SAS programs to produce data sets, raw and analysis
- Under the guidance of a statistical programmer or biostatistician, understand how existing macros (reusable code) work and update them if needed
- Provide programming support to data management to detect database issues and provide reports to aid data review
- Follow good programming practices including writing code that is understandable, commented, and easy to modify
- Follow current PROMETRIKA and/or Sponsor Guidelines
- Under guidance of statistical programmer or biostatistician, convert datasets received in other formats to SAS datasets
- Understand and follow all applicable PROMETRIKA standard operating procedures (SOPs) as well as any client’s work instructions/SOPs that may apply to projects
- Perform other duties as assigned