Senior Manager Clinical Operations

JR United Kingdom; England; On-site; GBP 60,000 - 90,000; Full time

Job summary

A leading company in the clinical research sector is seeking a Senior Manager in Clinical Operations to lead global clinical studies primarily in Oncology. This role involves hands-on leadership in managing study timelines, budgets, and ensuring compliance with regulatory standards. The ideal candidate will have a strong background in clinical operations, particularly in Oncology, and will thrive in a fast-paced environment. This position offers a hybrid working model and a competitive salary package.

Benefits

Opportunity to work on innovative studies with global reach

Hybrid working (Hatfield-based office)

Competitive salary and benefits package

Chance to be part of a growing team making an impact in oncology research

Qualifications

• 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.

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.

Skills

Oncology

Communication

Problem-solving

Risk assessment

Job description

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Senior Manager Clinical Operations, hertfordshire

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Client:

Cpl Life Sciences

Location:

hertfordshire, United Kingdom

Job Category:

Other

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EU work permit required:

Yes

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Job Views:

2

Posted:

23.05.2025

Expiry Date:

07.07.2025

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Job Description:

About the Role:

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.