Are you looking to join a company where your contributions truly matter, and where you'll be part of a supportive, innovative team? MMS is a award-winning, data-focused clinical research organization (CRO). We pride ourselves on being a Great Place to Work certified organization, recognized for our exceptional culture and industry best employee retention rate. We support the pharmaceutical, biotech, and medical device industries with our proven, scientific approach to complex trial data and regulatory submission challenges. With a global footprint across four continents, MMS not only maintains an industry-leading customer satisfaction rating but also fosters a collaborative and inclusive work setting where employees can thrive. Join us at MMS and be part of a team that is shaping the future of clinical research.
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Job Description
- Mastery in generating tables, listings, and graphs from clinical trial databases using SAS.
- Utilizes System Development Life Cycle (SDLC) for programming deliverables.
- Advanced user in SAS programming, SAS Base, and SAS Macros. •Advanced knowledge of E-Submission Standards, Guidelines and Regulations.
- Mastery and train on SDTM standards including ability to write specifications.
- Advanced knowledge of ADaM standards including supporting specification writing.
- Proficient with MS Office applications.
- Advance knowledge of ICH, 21CRF Part 11, and ISO 9001:2000 requirements.
- Advanced experience with pooling of data sets for submissions.
- Advanced experience with BIMO outputs, define.xml, Reviewer's Guides, SDSP.
- Lead study or small programming project teams
- Independently manages tasks and projects to achieve set objectives. Provides guidance to more junior level colleagues.
- Identifies and suggests opportunities for improvement related to Service and/or Service Line at the
📌 Senior Statistical Programmer (Bengaluru)
🏢 MMS
📍 Bengaluru