Senior Biostatistics Lead, Clinical Trials

Senior Biostatistics Lead, Clinical Trials

Full-Time 60000 - 80000 Β£ / year (est.) No working from home possible
F. Hoffmann-La Roche AG

At a Glance

  • Tasks: Lead statistical design and analysis for impactful clinical trials.
  • Company: Join F. Hoffmann-La Roche AG, a leader in healthcare innovation.
  • Benefits: Competitive salary, health benefits, and opportunities for professional growth.
  • Other info: Collaborative environment with a focus on innovation and teamwork.
  • Why this job: Make a real difference in healthcare by ensuring trial integrity.
  • Qualifications: MSc or PhD with clinical trial experience and SAS or R proficiency.

The predicted salary is between 60000 - 80000 Β£ per year.

F. Hoffmann-La Roche AG is seeking a Senior Statistician in Welwyn to drive statistical integrity in clinical trials. You will be responsible for the design, conduct, and analysis of trials, ensuring rigorous results that contribute to regulatory submissions.

The ideal candidate holds an MSc or PhD and has clinical trial experience within pharmaceutical settings. This position requires proficiency in SAS or R, along with excellent communication skills to convey complex statistical concepts clearly.

The role promotes collaboration across teams and presents a unique opportunity to impact healthcare innovation.

Senior Biostatistics Lead, Clinical Trials employer: F. Hoffmann-La Roche AG

F. Hoffmann-La Roche AG is an exceptional employer, offering a dynamic work culture that fosters collaboration and innovation in the heart of Welwyn. Employees benefit from comprehensive professional development opportunities, competitive remuneration, and a commitment to advancing healthcare solutions, making it a rewarding place for those passionate about making a difference in clinical trials.

F. Hoffmann-La Roche AG

Contact Details:

F. Hoffmann-La Roche AG Recruitment Team

We think you need these skills to ace Senior Biostatistics Lead, Clinical Trials

Statistical Analysis
Clinical Trial Design
SAS
R
Regulatory Submissions
Communication Skills
Collaboration