Senior & Principal Statistical Programmers

R&D Partners; Birmingham; On-site; GBP 80,000 - 100,000; Full time

Job summary

A specialized clinical research organization in Birmingham seeks experienced Senior and Principal Statistical Programmers. You will lead SAS programming efforts for statistical analysis in clinical trials, ensure compliance with guidelines, and mentor junior programmers. Applicants must have the right to work in the UK and relevant experience in Statistical Programming within life sciences. This position is an exciting opportunity to shape the future of clinical programming in a growing CRO.

Qualifications

• Full right to work in the UK/EU is mandatory.
• Experience in Statistical Programming within Pharma, Biotech, CRO, or Medical Device sectors.

Responsibilities

• Lead the design, development, and validation of SAS programs for clinical trial data analysis.
• Collaborate with biostatisticians on analysis plans and statistical methods.
• Conduct quality checks on statistical outputs for compliance.
• Assist in preparing statistical reports and regulatory submissions.
• Mentor junior programmers and share technical knowledge.

Skills

Statistical Programming

Communication skills

Collaboration with biostatisticians

Job description

Lead the code behind clinical breakthroughs-join a CRO investing in the future of Statistical Programming.

R&D Partners is seeking Senior and Principal Statistical Programmers to join a highly specialized CRO that is investing heavily in the growth of its Statistical Programming function.

Please note that to be considered for this role you must have the right to work in this location.

Responsibilities :

• Lead / support the design, development and validation of SAS programs for statistical analysis and reporting of clinical trial data
• Collaborate closely with biostatisticians to create comprehensive analysis plans and apply appropriate statistical methods.
• Perform QC checks and review statistical outputs to ensure compliance with project specifications and regulatory guidelines.
• Assist in the preparation of statistical reports, presentations, and regulatory submissions to support clinical development programs.
• Mentor junior programmers and contribute to team development by sharing best practices and technical knowledge.

Key Skills and Requirements :

• Full right to work in UK / EU
• Experience in Statistical Programming within a Pharma, Biotech, CRO, Medical Device or similar company
• Skilled communicator to Statistical Programming and Non-Statistical Programming personnel

For more information, please contact George Breen.

If you are interested in applying to this exciting opportunity, then please click 'Apply' or to speak to one of our specialists visit the 'Contact Us' page.

R&D Partners is a leading life sciences recruiter focused on finding exceptional people and matching them with the finest positions across the globe. R&D Partners is acting as an Employment Agency in relation to this vacancy.

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