Senior Manager, Clinical Programming

A company is looking for a Senior Manager, Clinical Programming.

Key Responsibilities

Develop and implement Study Data Tabulation Model (SDTM) standards ensuring compliance with industry standards

Ensure alignment of SDTM standards with data collection standards and provide SDTM mapping guidance

Serve as a subject matter expert on standards development and facilitate continuous process improvement

Required Qualifications

Bachelor's degree in Statistics, Computer Science, or Life Sciences; Master's degree preferred

At least 6-8 years of relevant experience in the pharmaceutical, biotech, CRO, or Regulatory Agency

Proficient in SAS programming with 6-8 years of experience

Practical knowledge of R to support clinical trials preferred

Demonstrated knowledge of clinical research, metadata management, and regulatory requirements