At a Glance
- Tasks: Lead statistical programming for clinical trials and oversee CRO contributions.
- Company: Join Cytel, a leader in clinical data solutions with a strong pharmaceutical partnership.
- Benefits: Competitive salary, flexible work options, and opportunities for professional growth.
- Other info: Be part of a dynamic team focused on innovation and compliance.
- Why this job: Make a significant impact on clinical trials while working with top-tier professionals.
- Qualifications: Extensive CDISC experience and expert SAS skills required.
The predicted salary is between 63000 - 77000 £ per year.
Cytel is seeking a Principal Statistical Programmer to operate within a sponsor-driven program embedded with a leading pharmaceutical client.
The role focuses on delivering high-quality statistical programming for clinical trials, with strong independence and leadership within a biometrics team.
You will oversee CRO contributions and ensure compliance with FDA/ICH guidelines.
The ideal candidate will have extensive CDISC experience (SDTM/ADa M/Define. xml), expert SAS skills, and a track record of
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Principal Statistical Programmer: Lead Clinical Data & Submissions employer: Cytel
Cytel is an exceptional employer that fosters a collaborative and innovative work culture, particularly for Biostatisticians dedicated to advancing Chemistry, Manufacturing, and Control (CMC) projects. With a strong emphasis on employee development, you will benefit from consistent training and support while working closely with a global pharmaceutical client at the forefront of patient treatment. This role offers the unique opportunity to contribute to meaningful projects in a dynamic environment where your expertise in Bayesian analysis can truly make an impact.
