Strategic Biostatistics Director, FSP for Clinical Trials in England

Strategic Biostatistics Director, FSP for Clinical Trials in England

England Full-Time 54000 - 66000 Β£ / year (est.) No working from home possible
IQVIA LLC

At a Glance

  • Tasks: Lead biostatistics strategy for clinical trials and shape study designs.
  • Company: Join IQVIA LLC, a leader in healthcare data and analytics.
  • Benefits: Competitive salary, flexible working options, and opportunities for professional growth.
  • Other info: Collaborative environment with cross-functional teams and regulators.
  • Why this job: Make a real impact on clinical trials and regulatory submissions.
  • Qualifications: Extensive experience in clinical trial statistics and advanced SAS/R programming.

The predicted salary is between 54000 - 66000 Β£ per year.

IQVIA LLC is seeking a Senior Biostatistician to lead the Biostatistics strategy for a therapeutic program, shaping study designs and analyses for regulatory submissions.

You will partner with cross-functional teams and interact with regulators to ensure high-quality results and timely delivery.

The role requires extensive experience in clinical trial statistics, advanced SAS/R programming, and a track record in regulatory submissions and strategic study design.

#J-18808-Ljbffr

Strategic Biostatistics Director, FSP for Clinical Trials in England employer: IQVIA LLC

IQVIA LLC is an exceptional employer located in the vibrant town of Livingston, Scotland, offering a dynamic work culture that prioritises scientific excellence and patient outcomes. Employees benefit from comprehensive training and development opportunities, fostering personal and professional growth within the clinical lab services sector. With a strong emphasis on teamwork and innovation, IQVIA provides a rewarding environment for those looking to make a meaningful impact in healthcare.

IQVIA LLC

Contact Details:

IQVIA LLC Recruitment Team

We think you need these skills to ace Strategic Biostatistics Director, FSP for Clinical Trials in England

Biostatistics
Clinical Trial Statistics
SAS Programming
R Programming
Regulatory Submissions
Study Design
Cross-Functional Collaboration