Senior Clinical Research Associate

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

Job summary

A small CRO is looking for a Senior Clinical Research Associate specializing in oncology trials. This role is remote with significant travel across the UK, primarily monitoring Phase I–III trials. Candidates need at least 4 years of CRA experience in oncology and a relevant bachelor's degree. The position requires compliance with ICH-GCP guidelines and offers a salary of up to £65,000 depending on experience. This position is ideal for someone based near London due to the site distribution.

Qualifications

• Minimum 4 years of on-site monitoring experience as a CRA in oncology.
• In-depth knowledge of ICH-GCP and regulatory guidelines.
• Must be based within 1 hour of a major airport or railway station.

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 across multiple UK locations.

Skills

Oncology clinical trials monitoring

Compliance with ICH-GCP

Study management

Data collection in clinical trials

Education

Bachelor’s degree in life sciences

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.