Global Clinical Study Lead β€” IVD Diagnostics in Manchester

Global Clinical Study Lead β€” IVD Diagnostics in Manchester

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

At a Glance

  • Tasks: Lead global clinical studies for innovative diagnostics in oncology and biopharma.
  • Company: Join QIAGEN, a leader in IVD solutions with a focus on innovation.
  • Benefits: Competitive salary, health benefits, and opportunities for professional growth.
  • Other info: Dynamic work environment with a focus on scientific excellence and career advancement.
  • Why this job: Make a real impact in healthcare by driving regulatory approval for cutting-edge diagnostics.
  • Qualifications: Experience in clinical study management and strong collaboration skills.

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

QIAGEN in the United Kingdom is hiring a Clinical Study Lead (CSL) to spearhead global clinical performance studies for our Oncology and Biopharma Companion Diagnostics portfolio, enabling regulatory approval of innovative IVD solutions. You will collaborate with pharmaceutical partners, clinical sites, and internal teams to deliver studies to high scientific, regulatory, and operational standards.

In this role, you will manage study design, start-up, conduct, and close-out, produce protocols.

Global Clinical Study Lead β€” IVD Diagnostics in Manchester employer: QIAGEN

QIAGEN is an exceptional employer that fosters a collaborative and innovative work culture, perfect for those passionate about advancing Life Science research. With a strong focus on employee growth, you will have access to ongoing training and development opportunities, alongside a competitive benefits package that includes private healthcare and flexible working options, making it an ideal place to thrive in the Midlands & South Wales region.

QIAGEN

Contact Details:

QIAGEN Recruitment Team

We think you need these skills to ace Global Clinical Study Lead β€” IVD Diagnostics in Manchester

Clinical Study Management
Regulatory Knowledge
Oncology Expertise
Biopharma Companion Diagnostics
Protocol Development
Collaboration Skills
Operational Standards