Senior Manager Clinical Operations

Cpl Life Sciences; England; Hybrid; GBP 70,000 - 90,000; Full time

Job summary

A leading company in the healthcare sector is seeking a (Senior) Manager, Clinical Operations to join their dynamic team. This role involves hands-on leadership in managing clinical studies primarily in Oncology, ensuring compliance with quality and regulatory standards. The ideal candidate will thrive in a fast-paced environment and contribute to innovative therapies. Key responsibilities include overseeing study timelines, budgets, and vendor performance, while collaborating with cross-functional teams. This position offers hybrid working and a competitive salary package.

Benefits

Competitive salary and benefits package

Opportunity to work on innovative studies with global reach

Hybrid working

Qualifications

• Minimum 5 years’ experience in clinical operations within pharma, biotech, or CRO.
• Strong background in Oncology clinical studies.

Responsibilities

• Lead and manage operational delivery of global/regional clinical studies.
• Ensure studies are conducted in accordance with ICH/GCP guidelines.

Skills

Communication

Problem Solving

Job description

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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

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
• 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.

Seniority level

• Seniority level

  Mid-Senior level

Employment type

• Employment type

  Full-time

Job function

• Job function

  Science

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