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# Principal Or Senior Statistical Programmer - Remote - Spain

- **Company:** Veramed
- **Location:** Cuenca, Spain (Remote available)
- **Contract:** Permanent contract
- **Skills:** Coherent Remote File System (CRFS), SAS (Software)
- **Published:** September 28, 2026
- **Apply:** https://www.buscojobs.com.es/principal-or-senior-statistical-programmer-remote-spain-en-cuenca-ID-372408326

## About the Role

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 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.

## Description

Ready for your next career move?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 is 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 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 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.