Senior Biostatistician: Lead Data-Driven Drug Development in Manchester

Senior Biostatistician: Lead Data-Driven Drug Development in Manchester

Manchester Full-Time 63000 - 77000 Β£ / year (est.) No working from home possible
MMS

At a Glance

  • Tasks: Lead statistical analyses and deliverables for drug development projects.
  • Company: MMS, a data-focused clinical research organisation in Manchester.
  • Benefits: Competitive salary, flexible working hours, and opportunities for professional growth.
  • Other info: Join a dynamic team dedicated to innovative healthcare solutions.
  • Why this job: Make a real impact on drug development with your statistical expertise.
  • Qualifications: Strong SAS programming skills and experience in clinical trials required.

The predicted salary is between 63000 - 77000 Β£ per year.

MMS, a data-focused clinical research organization, seeks a Senior Biostatistician in Manchester to lead statistical analyses and deliverables across drug development programs. You will apply strong SAS programming, CDISC SDTM/ADaM expertise, and clinical trial experience to support sponsor collaborations and regulatory submissions.

You will review ADAM/TLFs, produce high-quality statistical outputs, and guide project teams on statistical methods and study design while maintaining compliance.

Senior Biostatistician: Lead Data-Driven Drug Development in Manchester employer: MMS

At MMS, we are committed to creating a workplace where your expertise as a Senior Statistical Programmer is valued and nurtured. Our Great Place to Work certification reflects our dedication to fostering a supportive and innovative culture, offering exceptional employee retention rates and opportunities for professional growth. Join us in our remote UK team and be part of a collaborative environment that not only prioritises your career advancement but also shapes the future of clinical research.

MMS

Contact Details:

MMS Recruitment Team

We think you need these skills to ace Senior Biostatistician: Lead Data-Driven Drug Development in Manchester

SAS Programming
CDISC SDTM
CDISC ADaM
Clinical Trial Experience
Statistical Analysis
Regulatory Submissions
Project Team Guidance