Clinical Operations Lead

Proclinical Staffing; Plymouth; On-site; GBP 50,000 - 75,000; Full time

Job summary

A leading life sciences recruiter is seeking a Clinical Operations Lead to oversee clinical studies in the UK. This pivotal role involves ensuring quality and compliance, managing site relationships, and leading a team of Clinical Research Associates to drive patient-centric practices.

Qualifications

• Strong background in clinical operations with direct site interaction experience.
• Proven leadership skills in delivering studies with quality and compliance.
• Understanding of the UK clinical trial landscape and regulatory environment.

Responsibilities

• Oversee the operational delivery of clinical studies from start-up to close-out.
• Manage site relationships and performance within the UK.
• Lead and support UK-based Clinical Research Associates.

Skills

Leadership

Strategic communication

Stakeholder engagement

Job description

2 days ago Be among the first 25 applicants

Direct message the job poster from Proclinical Staffing

Ready to lead projects that bring life-changing treatments to the world? Join our client at the forefront of pharmaceutical innovation and make a difference!

Proclinical is seeking a Clinical Operations Lead to oversee the operational delivery of clinical studies in the UK. This role involves ensuring quality, compliance, and performance across all phases of clinical trials. You will be pivotal in managing site relationships and leading a team of Clinical Research Associates, focusing on patient-centric and inclusive practices.

Please note that to be considered for this role you must have the right to work in this location or hold an EU passport.

Responsibilities:

• Oversee the operational delivery of clinical studies from start-up to close-out.
• Represent the UK in global study teams, driving timelines and recruitment.
• Manage site relationships and performance within the UK.
• Lead and support UK-based Clinical Research Associates.
• Collaborate with local Medical Affairs and colleagues for alignment on start-up and execution.
• Ensure compliance with ICH-GCP, SOPs, and regulatory requirements.
• Lead study risk management, budget oversight, and diversity plans.
• Support responses to IRB/IEC/Health Authority queries and audits.

Key Skills and Requirements:

• Strong background in clinical operations with direct site interaction experience.
• Proven leadership skills in delivering studies with quality and compliance.
• Strategic communication and stakeholder engagement capabilities.
• Understanding of the UK clinical trial landscape and regulatory environment.
  

If you are having difficulty in applying or if you have any questions, please contact Joshua Bye at [e-mail].

If you are interested in applying to this exciting opportunity, then please click 'Apply' or to speak to one of our specialists please request a call back at the top of this page.

Proclinical is a leading life sciences recruiter focused on finding exceptional people and matching them with the finest positions across the globe. Proclinical is acting as an Employment Agency in relation to this vacancy.

By submitting this application, you confirm that you've read and understood our privacy policy, which informs you how we process and safeguard your data - https://www.proclinical.com/privacy-policy.

Seniority level

• Seniority level

  Mid-Senior level

Employment type

• Employment type

  Full-time

Job function

• Job function

  Science

• Industries

  Professional Services

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