Senior Clinical Research Associate

JR United Kingdom; London; On-site; GBP 40,000 - 70,000; Full time

Job description

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Senior Clinical Research Associate, london

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Client:

CCS-Global

Location:

london, United Kingdom

Job Category:

Other

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EU work permit required:

Yes

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Job Views:

5

Posted:

24.04.2025

Expiry Date:

08.06.2025

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Job Description:

Clinical Research Associates – Senior & Lead CRA London + Southern United Kingdom.

About the Company

CCS Global is partnering with a highly regarded leader in clinical research as they expand their team. We are actively seeking experienced Clinical Research Associates ( Senior CRA, and Lead CRA levels) across London and the South of the UK to support innovative and complex clinical trials.

Our client is recognised for their commitment to advancing clinical research and improving patient outcomes. If you’re looking for a role with a forward-thinking organisation that values expertise, career development, and quality-focused monitoring, this could be your next opportunity.

About the Role

As a Clinical Research Associate, you will act as the key liaison between study sites, sponsors, and regulatory bodies, ensuring the successful delivery of clinical trials across the UK. You will work across a range of therapeutic areas, including oncology, cardiology, CNS, medical devices, and rare diseases, with opportunities to gain experience in complex trials, including gene therapy studies.

What’s on Offer?

• Broad Therapeutic Exposure – Work across multiple indications, expanding your expertise and career potential.
• Career Progression – A structured development path with opportunities for advancement at all levels.
• Thoughtful Site Allocation – A strategic approach to site visits and local study site allocation, prioritizing quality over volume.
• Comprehensive Training – Access to top-tier training programs to keep you at the forefront of clinical research.

Key Responsibilities

• Independently monitor and oversee clinical trials in line with ICH-GCP and regulatory standards.
• Work closely with site teams to ensure high-quality and compliant study execution.
• Contribute to site selection and feasibility assessments.
• Provide mentorship to junior CRAs (for senior and lead-level roles).
• Support protocol development and study management activities as needed

Who We’re Looking For

• A Senior CRA, or Lead CRA with a minimum of 3.5 years’ independent monitoring experience.
• Strong knowledge of the UK clinical research landscape and regulatory environment.
• A valid UK driver’s license and full right to work in the UK.
• Excellent communication, organisational, and documentation skills.

If you’re looking for a role where you can develop your career, work on impactful studies, and be part of a supportive team, we’d love to hear from you.

Apply now with your updated CV, and we’ll be in touch.