Associate Director, Clinical Operations - Rare Disease

Associate Director, Clinical Operations - Rare Disease

Full-Time 63000 - 77000 Β£ / year (est.) No working from home possible
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At a Glance

  • Tasks: Lead clinical trials and collaborate with various teams to drive rare disease programmes.
  • Company: Eblex Group, a dynamic biotech company focused on rare diseases.
  • Benefits: Competitive salary, flexible working, and opportunities for professional growth.
  • Other info: Fast-paced environment with a focus on innovation and collaboration.
  • Why this job: Make a real difference in patients' lives while advancing your career in biotech.
  • Qualifications: Experience in clinical operations and strong leadership skills required.

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

Eblex Group is seeking an Associate Director of Clinical Operations to drive delivery of its rare disease clinical programmes in a lean biotech setting.

You will collaborate with Clinical Development, Medical, Regulatory, CMC, Quality and external partners to move studies from planning through completion.

This hands-on role requires leadership of clinical trials, strong protocol development, and experience managing CROs in a fast-moving biotech environment.

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Associate Director, Clinical Operations - Rare Disease employer: Eblex Group

Eblex Group offers an exceptional opportunity for the Associate Director, Clinical Operations role within a dynamic and innovative rare disease biotech. With a strong emphasis on collaboration and cross-functional teamwork, employees benefit from a supportive work culture that fosters professional growth and development. Located in a fast-paced environment, this position allows for meaningful contributions to clinical development programmes, making it an attractive choice for those seeking impactful and rewarding employment.

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Contact Details:

Eblex Group Recruitment Team

We think you need these skills to ace Associate Director, Clinical Operations - Rare Disease

Leadership of Clinical Trials
Protocol Development
CRO Management
Collaboration with Clinical Development
Collaboration with Medical Teams
Collaboration with Regulatory Affairs
Collaboration with CMC