At a Glance
- Tasks: Lead and support clinical trials, ensuring statistical integrity and regulatory compliance.
- Company: Cytel, a leader in biostatistics and clinical trial support.
- Benefits: Competitive salary, flexible work options, 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 leading impactful clinical studies.
- Qualifications: 5+ years of experience in clinical trials and strong SAS/R programming skills.
The predicted salary is between 59400 - 72600 £ per year.
Cytel is seeking a Senior Biostatistician to support or lead Phase I–IV clinical studies, embedded with a pharmaceutical client.
You will provide statistical leadership, develop SAPs, design studies, and ensure regulatory submissions meet CDISC and FDA guidelines.
Ideal candidates bring 5+ years of trial experience, SAS and R programming skills, and a strong ability to communicate complex statistics to non-statisticians.
Collaboration across CROs and internal teams is essential.
Senior Biostatistician - Clinical Trials Lead (Phase I-IV) in London employer: Cytel
Cytel is an exceptional employer that empowers its employees to thrive in a collaborative and innovative environment, particularly for the role of Principal SAS Programmer. With a strong commitment to professional development and training, Cytel ensures that you have the support needed to excel in your career while working remotely with a leading global pharmaceutical client. The company values diversity of thought and encourages autonomy, making it an ideal place for those looking to make a meaningful impact in the field of clinical trials.
