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- Tasks: Lead and manage global clinical studies in Oncology, ensuring quality and compliance.
- Company: Join a dynamic team focused on developing innovative therapies in the healthcare sector.
- Benefits: Enjoy hybrid working, competitive salary, and a comprehensive benefits package.
- Why this job: Make a real impact in oncology research while thriving in a fast-paced environment.
- Qualifications: 5+ years in clinical operations with a strong background in Oncology studies required.
- Other info: Mentorship opportunities available; no direct line management involved.
The predicted salary is between 54000 - 84000 £ per year.
We are seeking a highly motivated and experienced (Senior) Manager, Clinical Operations to join a dynamic Clinical Operations team. This role will take a hands-on leadership position in managing and executing clinical studies, primarily in Oncology, ensuring milestones and deliverables are met to the highest standards of quality, timelines, and regulatory compliance. This is an excellent opportunity for someone who thrives in a fast-paced, cross-functional environment and wants to contribute meaningfully to the development of innovative therapies.
Key Responsibilities:
- Lead and manage the operational delivery of one or more global/regional clinical studies (Phase I–III)
- Oversee study timelines, budgets, site selection, and vendor performance
- Ensure studies are conducted in accordance with ICH/GCP guidelines and applicable regulatory requirements
- Collaborate with cross-functional teams including medical, regulatory, and data management
- Participate in inspection readiness and co-monitoring activities as needed
- Mentor junior team members (no direct line management)
What We’re Looking For:
- Minimum 5 years’ experience in clinical operations within a pharma, biotech, or CRO environment
- Strong background in Oncology clinical studies
- Demonstrated success in managing global or regional trials from initiation through close-out
- Experience working with CROs and external vendors
- Strong knowledge of ICH/GCP and clinical regulatory landscape
- Excellent communication and problem-solving skills
Desirable Attributes:
- Experience in Cardiovascular or Nephrology trials
- Ability to assess risks and implement creative, compliant solutions
- A collaborative mindset and a proactive, hands-on approach to trial delivery
What’s on Offer:
- Opportunity to work on innovative studies with global reach
- Hybrid working (Hatfield-based office)
- Competitive salary and benefits package
- A chance to be part of a growing team making an impact in oncology research
Ready to take the lead on meaningful trials? Apply now or reach out for a confidential discussion.
Senior Manager Clinical Operations employer: Cpl Life Sciences
Contact Detail:
Cpl Life Sciences Recruiting Team
StudySmarter Expert Advice 🤫
We think this is how you could land Senior Manager Clinical Operations
✨Tip Number 1
Familiarise yourself with the latest trends and developments in Oncology clinical studies. This will not only help you understand the current landscape but also demonstrate your passion and commitment to the field during discussions.
✨Tip Number 2
Network with professionals in the clinical operations space, especially those who have experience in managing global trials. Engaging with industry peers can provide valuable insights and potentially lead to referrals.
✨Tip Number 3
Prepare to discuss specific examples of how you've successfully managed timelines, budgets, and vendor performance in past roles. Being able to articulate your hands-on experience will set you apart from other candidates.
✨Tip Number 4
Showcase your leadership skills by highlighting any mentoring or coaching experiences you've had with junior team members. This aligns well with the role's requirement for a collaborative mindset and proactive approach.
We think you need these skills to ace Senior Manager Clinical Operations
Some tips for your application 🫡
Tailor Your CV: Make sure your CV highlights relevant experience in clinical operations, particularly in Oncology. Emphasise your leadership roles and any specific achievements in managing clinical studies.
Craft a Compelling Cover Letter: Write a cover letter that showcases your passion for clinical research and your understanding of the role. Mention specific experiences that align with the job responsibilities, such as managing global trials or working with CROs.
Highlight Regulatory Knowledge: In your application, clearly demonstrate your knowledge of ICH/GCP guidelines and regulatory requirements. Provide examples of how you've ensured compliance in past projects.
Showcase Collaboration Skills: Since the role involves working with cross-functional teams, include examples of successful collaborations in your application. Highlight your communication skills and ability to work in a fast-paced environment.
How to prepare for a job interview at Cpl Life Sciences
✨Showcase Your Oncology Expertise
Make sure to highlight your experience in Oncology clinical studies during the interview. Be prepared to discuss specific trials you've managed and the outcomes, as this will demonstrate your relevant knowledge and skills.
✨Demonstrate Leadership Skills
As a Senior Manager, you'll need to show that you can lead and mentor teams effectively. Share examples of how you've successfully managed teams or projects, focusing on your hands-on approach and ability to drive results.
✨Familiarise Yourself with ICH/GCP Guidelines
Since compliance is crucial in clinical operations, brush up on ICH/GCP guidelines before the interview. Be ready to discuss how you've ensured adherence to these standards in past projects, as this will reflect your commitment to quality.
✨Prepare for Cross-Functional Collaboration Questions
Expect questions about your experience working with cross-functional teams. Prepare examples that illustrate your collaborative mindset and how you've effectively communicated with different departments to achieve study goals.
