Senior Clinical Research Associate

This range is provided by CCS-Global. Your actual pay will be based on your skills and experience — talk with your recruiter to learn more.

Base pay range

Direct message the job poster from CCS-Global

Senior/Lead Clinical Research Associate (CRA) – Remote in the United Kingdom

Are you an experienced CRA looking for your next significant step? Do you thrive in an environment that values a thoughtful approach to site management and prioritises employee well‑being? If so, we have a great opportunity for you to join a leading team in the UK.

The client, a global CRO, are seeking a highly motivated Senior or Lead CRA to contribute to the advancement of ground‑breaking therapies across a range of compelling areas, including Oncology, Haemato‑oncology, Rare Diseases, and other innovative fields. You will play a crucial role in ensuring the smooth and efficient conduct of clinical trials, working with a network of more localised sites.

What sets the team apart?

• Focus on Quality, Not Just Metrics: The team champions a solid thought process in site management, understands that effective collaboration and proactive problem‑solving are paramount, and fosters trust in their CRAs to manage sites without the burden of a rigid minimum number of days on site.
• Genuine Career Development: The organisation is deeply invested in the growth of its team members, offering clear pathways for career progression with ongoing training and mentorship opportunities.
• Exceptional Team Retention: A supportive, engaging work environment that values and empowers individuals, with a commitment to clear communication, work‑life balance, and recognition of contributions.
• Meaningful Employee Engagement: Your insights help shape integral processes and contribute to a positive, productive workplace, a cornerstone of long‑term success.

As a Senior/Lead CRA, your responsibilities will include:

• Independently managing all aspects of site monitoring, from initiation to close‑out.
• Building and maintaining strong relationships with investigators and site staff.
• Ensuring adherence to study protocols, Good Clinical Practice (GCP), and relevant regulatory requirements.
• Contributing to the development of study‑related documents.
• Mentoring and supporting junior CRAs (for Lead level).

To be successful in this role, you will have:

• Significant independent monitoring experience within clinical research.
• A strong understanding of GCP and relevant regulations.
• Excellent communication, organisation, and problem‑solving skills.
• A proactive and detail‑oriented approach.
• Experience in one or more of the aforementioned therapeutic areas (Oncology, Haemato‑oncology, Rare Diseases) is highly desirable.

If you are looking for a rewarding career where your expertise is valued, your professional development is prioritised, and you can contribute to the advancement of truly innovative medicines, we encourage you to apply.

To Apply:

Please submit your CV and a covering letter outlining your relevant experience and why you are interested in this opportunity.

Seniority level

Mid‑Senior level

Employment type

Full‑time

Job function

Project Management

Industries

Biotechnology Research, Health and Human Services, and Pharmaceutical Manufacturing