Senior Clinical Research Associate

RBW Consulting; Remote; GBP 55,000 - 65,000; Full time

Job summary

A small clinical research organization is seeking a Senior Clinical Research Associate to monitor oncology trials across the UK. This home-based role requires candidates with over 4 years of CRA experience and expertise in ICH-GCP. You will manage studies and conduct site visits to ensure compliance. A Bachelor's degree in life sciences is essential, alongside a valid driver's license. The position involves significant UK travel, making it ideal for candidates based near London.

Qualifications

• Minimum 4 years of on-site monitoring as a CRA, with a strong track record in oncology.
• In-depth knowledge of ICH-GCP and regulatory guidelines.
• Valid driver's license and passport preferred.

Responsibilities

• Monitor Phase I–III oncology clinical trials across UK sites.
• Conduct site visits ensuring compliance with ICH-GCP and regulatory requirements.
• Manage 1–3 studies concurrently, overseeing multiple sites.

Skills

Oncology clinical trials monitoring

Compliance with ICH-GCP

Cross-functional collaboration

Education

Bachelor's degree in life sciences or related field

Job description

Job Details

• Job Title : Senior Clinical Research Associate (Oncology)
• Location : UK, Remote
• Other Details : Full-Time | Permanent | Small CRO
• Salary : Up to £65,000 (DOE)

Are you an experienced CRA with a strong background in oncology trials? A small, agile CRO is seeking a Senior Clinical Research Associate to join their growing team. This is a home‑based role with national travel, where half the sites are based in London.

Key Responsibilities

• Monitor Phase I–III oncology clinical trials across UK sites.
• Conduct site visits (approx. 6–7 days / month) ensuring compliance with ICH‑GCP and regulatory requirements.
• Manage 1–3 studies concurrently, overseeing 4–7 sites located in London, Manchester, Glasgow, Liverpool, Sheffield, and Cardiff.
• Apply RECIST criteria confidently in oncology assessments.
• Collaborate with cross‑functional teams to ensure high‑quality data collection and trial conduct.

Candidate Profile

• Experience: Minimum 4 years of on‑site monitoring as a CRA, with a strong track record in oncology (Phase I–III).
• Education: Bachelor’s degree (BSc, BA, or RN equivalent) in a life sciences or related field.
• In‑depth knowledge of ICH‑GCP and regulatory guidelines.
• Location: Must be based within 1 hour of a major airport or railway station. Preference for candidates located in or near London due to site distribution.
• Travel: Up to 70% travel across the UK; valid driver’s license and passport preferred.

To apply:

Please click ‘apply’ or contact Joe Pearce for any further information.

Equal Opportunities Statement

We are an equal opportunities Recruitment Business and Agency. RBW Consulting is an equal opportunity workplace. We prioritize talent (both current and potential) over resumes, challenge the status quo, and value people as our most important asset. We do not discriminate on the basis of race, ethnicity, colour, sex, gender identity or expression, sexual orientation, religion, age, marital status, visible or invisible disability, medical condition, national origin, veteran status, or any other protected status. We strive to be a diverse workforce that is representative at all levels and are committed to building a team that represents a variety of backgrounds, perspectives, and skills.