Veramed
Principal or Senior Statistical Programmer - Remote or Hybrid - UK
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With continued business growth and a strong pipeline of new projects, Veramed is creating new opportunities for Statistical Programmers to work on innovative studies, expand their skills, and advance their careers within a supportive, specialist CRO.
We have multiple exciting opportunities
For Principal and Senior level Statistical Programmers skilled in SAS and R, to join us on a permanent basis. We can offer fully remote, hybrid, or office-based working, training, and a very supportive and quality-focused environment.
The purpose of the role
To provide programming support to the statistics and programming department across a range of projects, clients, and therapeutic areas. The Senior or Principal Programmer may also perform a supervisory role (e.g. line management and/or project management).
Key Responsibilities
Technical
- Previous experience with SAS and some R experience/knowledge.
- Perform 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 programming practice.
- Identify data issues and outliers.
- Complete, review, and approve CDISC Validation tool reports.
- Identify data and standards issues and resolve or escalate 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.
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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.
- Lead process improvement initiatives.
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Minimum Qualification Requirements
- 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 both 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.
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