Eblex Group is supporting a growing rare disease biotech in the search for an Associate Director, Clinical Operations to support the delivery of its clinical development programmes.
This is a broad, hands on role within a lean biotech environment, working closely with Clinical Development, Medical, Regulatory, CMC, Quality and external partners to deliver clinical studies from planning through to completion.
Key Responsibilities as Associate Director, Clinical Operations
- Lead clinical operations across assigned rare disease clinical trials
- Support protocol development, feasibility and operational strategy
- Develop study timelines, budgets and operational plans
- Lead CRO selection, oversight and vendor management
- Develop site and patient recruitment strategies for challenging rare disease populations
- Oversee study delivery, risks, milestones and quality
- Ensure compliance with ICH GCP and applicable global regulations
- Work cross functionally across Clinical, Medical, Regulatory, CMC, Quality and Data
- Support inspection readiness and TMF oversight
What We're Looking For in a Associate Director, Clinical Operations
- 8+ years' experience in clinical operations within biotech, pharma or CRO
- Strong experience leading clinical trials
- Previous rare disease experience highly desirable
- Strong understanding of ICH GCP and global clinical development
- Experience managing CROs and external vendors
- Comfortable working in a small, fast moving biotech environment
- Strong protocol development and operational planning experience
This is an opportunity to join a growing rare disease biotech where Clinical Operations will have a direct influence on development strategy and programme delivery.
Eblex Group is managing this search exclusively. Apply directly or contact us for a confidential discussion.
Clinical Operations | Clin Ops | Biotech | Rare Disease | Clinical | Associate Director, Clinical Operations | Global | Early Phase | Late Phase | Clinical Development
Associate Director Clinical Operations in London employer: Eblex Group
Eblex Group offers an exceptional work environment for Clinical Study Managers, providing the opportunity to thrive in a dynamic and supportive biotech setting focused on rare diseases. With a strong emphasis on collaboration across various departments and external partners, employees benefit from a culture that prioritises innovation, professional growth, and meaningful contributions to life-changing clinical programmes. The company's commitment to excellence ensures that team members are equipped with the resources and support needed to excel in their roles while making a significant impact in the field of biotechnology.
