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Principal or Senior Statistical Programmer - Remote -… - Jobeax

Principal or Senior Statistical Programmer - Remote - Spain en Madrid, España is listed on Jobeax. Browse 80,000+ vacancies available.

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

La experiencia que se espera de los solicitantes, así como las habilidades y cualificaciones adicionales necesarias para este trabajo, se enumeran a continuación.
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. xqysrnh

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