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- Tasks: Lead global oncology clinical trials and ensure high-quality delivery across multiple programmes.
- Company: Dynamic biotech company focused on innovative cancer treatments.
- Benefits: Competitive salary, comprehensive health benefits, and opportunities for professional growth.
- Why this job: Make a significant impact in oncology while collaborating with top industry professionals.
- Qualifications: 12+ years in clinical operations with extensive oncology trial experience.
- Other info: Join a supportive team that values innovation and patient safety.
The predicted salary is between 72000 - 108000 £ per year.
The Senior Director, Clinical Operations will provide strategic and operational leadership for the planning and execution of global oncology clinical trials, with primary accountability for UK and European clinical operations. This role is responsible for ensuring high-quality, compliant, and efficient trial delivery across multiple programs, working closely with CRO partners and internal cross-functional teams.
Key Responsibilities:
- Clinical Trial Leadership
- Lead the operational strategy and execution of global oncology clinical trials, including early- and late-stage studies.
- Provide oversight of UK and EU trial activities from start-up through close-out.
- Ensure delivery against timelines, budgets, and quality expectations while maintaining patient safety and data integrity.
- CRO & Vendor Oversight
- Own end-to-end CRO and vendor oversight for assigned studies and regions.
- Lead CRO selection, contracting, governance, and performance management.
- Establish clear KPIs, escalation pathways, and risk mitigation strategies appropriate for an outsourced model.
- Oncology & Cross-Functional Collaboration
- Partner closely with Clinical Development, Medical Affairs, Regulatory Affairs, Biometrics, Pharmacovigilance, and Quality.
- Contribute operational input to oncology protocol design, feasibility assessments, site selection, and enrollment strategies.
- Support regulatory interactions and inspections (MHRA, EMA, FDA as applicable).
Qualifications & Experience:
- Bachelor’s degree in life sciences or related discipline (advanced degree preferred).
- 12+ years of progressive experience in clinical operations within biotech and/or CRO environments.
- Extensive oncology clinical trial experience, including global, multi-site studies.
- Demonstrated success working in outsourced, CRO-led operating models.
- Strong knowledge of UK, EU, and global clinical trial regulations and ICH-GCP.
- Proven people leadership experience and ability to manage complex external partnerships.
- Excellent communication, organizational, and stakeholder-management skills.
Senior Director Clinical Operations in London employer: Discover International
Contact Detail:
Discover International Recruiting Team
StudySmarter Expert Advice 🤫
We think this is how you could land Senior Director Clinical Operations in London
✨Tip Number 1
Network like a pro! Reach out to your connections in the clinical operations field, especially those who have experience with oncology trials. A friendly chat can lead to insider info about job openings or even referrals.
✨Tip Number 2
Prepare for interviews by brushing up on your knowledge of UK and EU clinical trial regulations. We want you to showcase your expertise in managing complex partnerships and CRO oversight during those crucial conversations.
✨Tip Number 3
Don’t just apply anywhere; focus on companies that align with your values and career goals. Check out our website for opportunities that match your skills in clinical operations and oncology – we’ve got some great roles waiting for you!
✨Tip Number 4
Follow up after interviews! A quick thank-you email can keep you top of mind and show your enthusiasm for the role. Let them know you’re keen to bring your leadership skills to their clinical operations team.
We think you need these skills to ace Senior Director Clinical Operations in London
Some tips for your application 🫡
Tailor Your CV: Make sure your CV reflects the specific skills and experiences that align with the Senior Director, Clinical Operations role. Highlight your oncology clinical trial experience and any leadership roles you've held in clinical operations.
Craft a Compelling Cover Letter: Your cover letter is your chance to shine! Use it to explain why you're passionate about clinical operations and how your background makes you the perfect fit for our team. Don’t forget to mention your experience with CROs and multi-site studies.
Showcase Your Achievements: When detailing your experience, focus on quantifiable achievements. Did you lead a project that came in under budget or ahead of schedule? We want to see those numbers that demonstrate your impact in previous roles!
Apply Through Our Website: We encourage you to apply directly through our website. It’s the best way for us to receive your application and ensures you’re considered for the role. Plus, it shows you’re keen on joining our team at StudySmarter!
How to prepare for a job interview at Discover International
✨Know Your Oncology Inside Out
Make sure you brush up on the latest trends and regulations in oncology clinical trials. Familiarise yourself with key terms and recent advancements, as this will show your passion and expertise in the field during the interview.
✨Demonstrate Leadership Experience
Prepare specific examples of how you've successfully led teams and managed complex projects in previous roles. Highlight your experience with CROs and vendor management, as this is crucial for the Senior Director position.
✨Showcase Your Strategic Thinking
Be ready to discuss your approach to developing operational strategies for clinical trials. Think about how you would handle timelines, budgets, and quality expectations, and be prepared to share your thought process with the interviewers.
✨Engage with Cross-Functional Collaboration
Since this role requires working closely with various departments, prepare to talk about your experiences collaborating with Clinical Development, Medical Affairs, and other teams. Share how you’ve contributed to protocol design and site selection in past projects.
