Associate Manager, Statistical Programming

MMS; Remote; GBP 60,000 - 80,000; Full time

Job summary

An innovative clinical research organization is seeking a remote Associate Manager, Statistical Programming to lead and mentor programming teams. Ideal candidates will have advanced SAS programming skills and a minimum of 5 years in statistical programming or clinical programming. In this role, you will manage team members, resolve client demands, and drive project success, contributing to a collaborative and inclusive work environment. Join us to shape the future of clinical research.

Qualifications

• Minimum of 5 years experience in statistical programming, clinical programming or similar field required.
• Ability to anticipate and effectively resolve potential problems with client demands.
• Proficiency with MS Office applications and SAS programming.

Responsibilities

• Lead study or small programming project teams.
• Line manages programming team members ensuring that everyone can reach their potential.
• Train and mentor less experienced team members.

Skills

Advanced user in SAS programming (SAS Base and SAS Macros)

Mastery and training on SDTM standards including ability to write specifications

Advanced knowledge of ADaM standards

Experience with pooling of data sets for submissions

Good communication skills

Education

BSc or above within Computer Science, Mathematics or related discipline

Tools

MS Office applications

SAS

Job description

Associate Manager, Statistical Programming United Kingdom (Remote) MMS • London, England, UK

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 an 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. 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. Join us at MMS and be part of a team that is shaping the future of clinical research.

Discover more about our exciting opportunities and why MMS is a great place to advance your career. Follow MMS on LinkedIn.

We are looking for a full‑time employee remotely based within the United Kingdom.

Job Specific Skills

• Mastery and training on 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 training on SDTM standards including ability to write specifications.
• Advanced knowledge of ADaM standards including supporting specification writing.
• Advanced experience with pooling of data sets for submissions.
• Advanced experience with BIMO outputs Reviewers Guides SDSP.
• Lead study or small programming project teams.

Job Requirements

• Educated to BSc or above within Computer Science, Mathematics or a Science related discipline.
• Minimum of 5 years experience in statistical programming, clinical programming or similar field required.
• Ability to anticipate and effectively resolve potential problems with client demands.
• Line manages programming team members ensuring that everyone can reach their potential and identify their areas of development.
• Train and mentor less experienced team members.
• Coach and encourage internal and external teams about best practices which bring additional value.
• Proficiency with MS Office applications.
• Hands‑on experience with clinical trial and pharmaceutical development preferred.
• 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.
• Familiarity with current ISO 9001 and ISO 27001 standards preferred.
• Familiarity with 21 CFR Part 11, FDA and GCP requirements.
• Basic understanding of CROs and scientific & clinical data/terminology & the drug development process.

If you have not received a response within 14 days of your application please consider your application unsuccessful.

Required Experience

Manager