Senior Programmer

Overview

MMS is an award-winning, data-focused clinical research organization (CRO). 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 maintains an industry-leading customer satisfaction rating and fosters a collaborative and inclusive work environment where employees can thrive.

Responsibilities

• Generate tables, listings, and graphs from clinical trial databases using SAS.
• Apply the System Development Life Cycle (SDLC) framework to programming deliverables.
• Lead study or small programming project teams.
• Work as an advanced SAS programmer using SAS Base and SAS Macros.
• Apply advanced knowledge of ADaM standards, including supporting specification writing.
• Be proficient with MS Office applications.
• Pool data sets for submissions.
• Experience with XML, Reviewer’s Guides, and SDSP.
• Hands-on experience with clinical trial and pharmaceutical development is preferred.
• Maintain a basic understanding of CROs and scientific and clinical data terminology and the drug development process.

Qualifications

• Minimum of 5 years’ experience in Statistical Programming or a similar field.
• Expert knowledge of scientific principles and concepts.
• Reputation as an emerging leader in the field with sustained performance and accomplishments.
• MS Office applications proficiency.
• Strong understanding of the drug development process and regulatory submission challenges.

Salary: GBP 50,000 – 70,000 per year

Experience: 5 years required

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