Senior Statistical Programmer - Remote (US)

MMS•, (Multiple States)
•Remote

About The Position

MMS is an award-winning, data-focused clinical research organization (CRO) that prides itself on being a Great Place to Work certified organization, recognized for its 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 environment where employees can thrive. Applicants must be legally authorized to work in the U.S. for any employer; we cannot sponsor visas (e.g., H-1B) or offer work authorization transfers at this time.

Requirements

  • Masters required for all Statistics roles.
  • Minimum of 5 years’ experience in Statistical Programming or similar field required.
  • Expert knowledge of scientific principles and concepts.
  • Reputation as emerging leader in field with sustained performance and accomplishment.
  • Proficiency with MS Office applications.
  • Good communication skills and willingness to work with others to clearly understand needs and solve problems.
  • Excellent problem-solving skills.
  • Good organizational and communication skills.
  • Basic understanding of CROs and scientific & clinical data/terminology, & the drug development process.

Nice To Haves

  • Hands-on experience with clinical trial and pharmaceutical development preferred.
  • Familiarity with current ISO 9001 and ISO 27001 standards preferred.
  • Familiarity with 21 CFR Part 11, FDA, and GCP requirements.

Responsibilities

  • Generating tables, listings, and graphs from clinical trial databases using SAS.
  • Utilizes System Development Life Cycle (SDLC) for programming deliverables.
  • Lead study or small programming project teams.
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