Principal or Senior Statistical Programmer - Remote, Office or Hybrid - UK

Principal or Senior Statistical Programmer – Remote, Office or Hybrid – UK

Permanent position offering home and/or office work, training and support, and a competitive package.

Overview

Veramed provides high‑standard data management, biostatistics and programming services to clinical trials. The Principal or Senior Statistical Programmer will provide programming support across a range of projects, clients and therapeutic areas, and may assume supervisory roles.

Key Responsibilities

Technical

• Previous experience with SAS and R.
• Review of clinical trial documents including protocols, SAPs, CRFs, CSRs.
• Author, review and approve study TFL shells and dataset specifications.
• Author, validate and document SAS programs for datasets, TFLs and macros, applying good
• Identify data issues and outliers.
• Complete, review and approve CDISC Validation tool reports.
• Identify data and standards issues and resolve or elevate as appropriate.
• Awareness of emerging standards and associated impact to ongoing and future planned trials.
• Maintain proficiency in SAS and awareness of developments.
• Maintain study master file documents and any other documents that are required to be audit ready.

General

• Lead internal and client study, project and cross‑functional team meetings effectively.
• Present study updates internally and at client meetings.
• Share scientific, technical and practical knowledge within the team and with colleagues.
• Perform work in full compliance with applicable internal and client policies, procedures, processes and training.
• Build effective collaborative working relationships with internal and client team members.
• Ensure learnings are shared across projects or studies.
• Develop and provide internal technical training where appropriate.
• BSc, MSc or PhD in numerical discipline (or relevant equivalent industry experience).
• At least 6 years of relevant industry experience.

Other Information / Additional Requirements

• Understanding of clinical drug development process, relevant disease areas, endpoints and study designs.

What to Expect

• A warm, friendly working environment in which to thrive personally and professionally.
• A supportive, open‑door management policy that will aid in your development and provide you with the tools to take your career to the next level.
• A truly unique CRO that’s doing something different when it comes to managing staff, projects and building relationships in the industry.
• The ability to own your role and develop your skills and experience.

Seniority Level

Mid‑Senior level

Employment Type

Full‑time

Job Function

Research and Science

Industries

Pharmaceutical Manufacturing