Senior Biostatistics Lead, Clinical Development in Maidenhead

Senior Biostatistics Lead, Clinical Development in Maidenhead

Maidenhead Full-Time 80000 - 100000 Β£ / year (est.) No working from home possible
CSL

At a Glance

  • Tasks: Lead statistical strategies for clinical trials and regulatory submissions.
  • Company: CSL, a leading biopharmaceutical company in Maidenhead.
  • Benefits: Attractive salary, comprehensive health benefits, and opportunities for professional growth.
  • Other info: Collaborative environment with a focus on innovation and excellence.
  • Why this job: Make a significant impact on clinical development and patient outcomes.
  • Qualifications: Strong background in biostatistics and experience in clinical trial design.

The predicted salary is between 80000 - 100000 Β£ per year.

CSL in Maidenhead, UK, seeks an Associate Director, Biostatistics to lead the statistical contribution across a clinical development program.

You will define strategies for trials and regulatory submissions, ensuring deliverables meet regulatory expectations and quality standards.

You will lead interactions with regulators, oversee internal and CRO statistical teams, and guide innovative study designs while communicating results to diverse stakeholders.

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Senior Biostatistics Lead, Clinical Development in Maidenhead employer: CSL

As an Associate Director in Procurement Enablement at CSL, you will be part of a forward-thinking organisation that prioritises sustainability and governance while fostering a culture of continuous improvement and talent development. With a commitment to employee growth through the Global Procurement Academy and a collaborative work environment, CSL offers a unique opportunity to influence procurement practices on a global scale, making it an excellent employer for those seeking meaningful and impactful careers.

CSL

Contact Details:

CSL Recruitment Team

We think you need these skills to ace Senior Biostatistics Lead, Clinical Development in Maidenhead

Statistical Analysis
Regulatory Submission Expertise
Clinical Trial Design
Leadership Skills
Communication Skills
Collaboration with CROs
Quality Assurance