Senior Clinical Research Associate

AL Solutions; Glasgow; Hybrid; GBP 45,000 - 55,000; Full time

Job summary

A leading global CRO is seeking an experienced Senior Clinical Research Associate to oversee clinical trials in England. The role involves managing site activities, ensuring compliance with ICH-GCP and UK regulations, along with providing guidance and support to site personnel. Ideal candidates should possess a Bachelor's degree in a relevant field and have at least three years of independent monitoring experience. This position offers competitive pay, flexible working arrangements, and growth opportunities within innovative therapy areas.

Benefits

Competitive salary

Flexible working arrangements

Career progression opportunities

Qualifications

• Minimum 3 years of independent UK monitoring experience.
• Exposure to complex studies preferred.
• Strong knowledge of ICH-GCP and UK clinical trial regulations.

Responsibilities

• Manage qualification, initiation, monitoring, and close-out visits.
• Perform source data verification and ensure accurate documentation.
• Identify site-level challenges and drive timely resolution.

Skills

Independent site monitoring

ICH-GCP compliance

Communication skills

Relationship-building

Organisational skills

Education

Bachelor's degree in Life Sciences, Nursing, Pharmacy, or a related discipline

Job description

Senior Clinical Research Associate – England

Chloe O’Shea is proud to partner with a leading global CRO renowned for delivering innovative, high-quality solutions in clinical development. We are seeking an experienced Senior Clinical Research Associate (Senior CRA) to join a dedicated single-sponsor team in England. This is an exciting opportunity to work on cutting‑edge studies, with a particular focus on advanced therapy areas such as CAR‑T and gene therapy. While prior experience in these fields is highly valued, it is not essential – full training and support will be provided.

The Role

As a Senior CRA, you will be a key contributor to the successful delivery of clinical trials across England. You will oversee site management activities, act as a primary liaison with investigative sites, and ensure strict compliance with protocols, ICH‑GCP, and UK regulatory requirements (MHRA / REC). This role is well‑suited to ambitious CRAs ready to step up or established Senior CRAs seeking to deepen their expertise in innovative therapy areas.

Key Responsibilities

• Independently manage qualification, initiation, monitoring, and close‑out visits across England.
• Ensure high standards of compliance with ICH‑GCP, MHRA, REC requirements, and sponsor SOPs.
• Perform source data verification, investigational product accountability, and ensure accurate site documentation.
• Serve as a trusted partner to site personnel, offering training, guidance, and ongoing support.
• Identify site‑level challenges proactively and drive timely resolution.
• Contribute to mentorship of junior CRAs and share best practices within the monitoring team.
• Maintain complete and accurate trial documentation in CTMS, eTMF, and EDC systems.

Requirements

• Bachelor’s degree in Life Sciences, Nursing, Pharmacy, or a related discipline.
• Minimum 3 years of independent UK monitoring experience, ideally with exposure to complex studies.
• Experience in CAR‑T and / or gene therapy is highly desirable but not required.
• Strong knowledge of ICH‑GCP and UK clinical trial regulations (MHRA / REC).
• Excellent communication, relationship‑building, and organisational skills.

What’s in It for You?

This role offers a competitive salary and benefits package, flexible working arrangements, and clear opportunities for career progression within one of the world’s largest CROs. You’ll gain exposure to innovative therapies shaping the future of healthcare, while working in a collaborative culture that values professional development, work‑life balance, and wellbeing.

If you are a driven Senior CRA — or an experienced CRA ready to take the next step — we’d love to hear from you. Apply today to join a global team making a meaningful difference in patients’ lives.