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

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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 upscale 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 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. xugodme

Hay opciones de teletrabajo/trabajo desde casa disponibles para este puesto.

📌 Principal or Senior Statistical Programmer - Remote (España)
🏢 Veramed
📍 España