At a Glance
- Tasks: Generate insightful data visuals and lead programming projects in clinical research.
- Company: Join an award-winning CRO with a global presence and a focus on collaboration.
- Benefits: Competitive salary, inclusive culture, and opportunities for professional growth.
- Other info: Dynamic work environment with a strong emphasis on employee satisfaction.
- Why this job: Make a real impact in the pharmaceutical industry while advancing your programming skills.
- Qualifications: 5+ years in Statistical Programming and expertise in SAS required.
The predicted salary is between 50000 - 70000 £ per year.
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 ADa M 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.
Experience: 5 years required
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Communication Skills
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