Lead Biostatistician & Associate Director, Clinical Trials

Lead Biostatistician & Associate Director, Clinical Trials

Full-Time 60000 - 80000 £ / year (est.) No working from home possible
Cytel

At a Glance

  • Tasks: Lead and design clinical studies while collaborating with diverse teams.
  • Company: Cytel, a leader in biostatistics and clinical trials.
  • Benefits: Competitive salary, professional growth, and a chance to impact healthcare.
  • Other info: Join a dynamic team and advance your career in a vital industry.
  • Why this job: Shape the future of drug development and enhance patient outcomes.
  • Qualifications: Master's or PhD in a relevant field with strong statistical skills.

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

Cytel is seeking a lead statistician for their clinical studies in the United Kingdom. The successful candidate will oversee phase I–IV studies, designing and reporting under senior supervision.

Responsibilities include collaborating with cross-functional teams to optimize study designs and timelines.

A strong background in statistical expertise, knowledge of drug development regulations, and proficiency in SAS and R programming is essential for this role. The ideal candidate will have a Master's or PhD in a relevant field and significant experience in the industry.

Lead Biostatistician & Associate Director, Clinical Trials employer: Cytel

Cytel is an exceptional employer that fosters a collaborative and innovative work culture, making it an ideal place for professionals in the biostatistics field. With a strong commitment to employee growth, Cytel offers numerous opportunities for advancement and skill development, particularly in the vibrant setting of the United Kingdom's clinical research landscape. Employees benefit from a supportive environment that values expertise and encourages contributions to impactful clinical studies.

Cytel

Contact Details:

Cytel Recruitment Team

We think you need these skills to ace Lead Biostatistician & Associate Director, Clinical Trials

Statistical Expertise
SAS Programming
R Programming
Knowledge of Drug Development Regulations
Study Design
Reporting Skills
Collaboration with Cross-Functional Teams