Negotiable
Undetermined
Hybrid
London Area, United Kingdom
Summary: The Senior Clinical Research Associate (CRA) role is a part-time contract position focused on a vascular medical device study in London, requiring approximately 2 days of work per week. The position involves hands-on monitoring, site engagement, and collaboration with internal teams to ensure high-quality study execution. The role offers the opportunity to work closely with senior leadership in a fast-paced, innovative environment. Candidates should have proven experience in clinical research within the medical device sector.
Key Responsibilities:
- Conduct monitoring visits and maintain strong site engagement
- Deliver light EDC training to study sites
- Support the generation and review of study documentation
- Provide remote oversight for additional UK and Irish sites
- Collaborate closely with internal teams to ensure high-quality study conduct
Key Skills:
- Proven Senior CRA experience within medical devices or relevant clinical research
- Strong monitoring and site management skills
- Confident communicator who can drive engagement across multiple sites
- Ability to work independently in a flexible, part-time arrangement
- Available to start January
Salary (Rate): undetermined
City: London
Country: United Kingdom
Working Arrangements: hybrid
IR35 Status: undetermined
Seniority Level: undetermined
Industry: Other
Senior CRA (Contract) – 0.4 FTE | Vascular Medical Device Study
Location: London (with occasional remote support for UK/Ireland sites)
Contract Length: 12 months
Start Date: January
FTE: 0.4 (Approx. 2 days per week)
About the Opportunity:
We are supporting an innovative medical device organisation developing next-generation endovascular technology . This specialist, fast-moving company operates with a lean structure, offering contractors the chance to work closely with senior leadership and make a tangible impact on study execution. This is an excellent opportunity for an experienced Senior Clinical Research Associate who enjoys hands-on involvement, autonomy, and contributing directly to the progress of a pivotal device study.
Key Responsibilities:
- Conduct monitoring visits and maintain strong site engagement
- Deliver light EDC training to study sites
- Support the generation and review of study documentation
- Provide remote oversight for additional UK and Irish sites
- Collaborate closely with internal teams to ensure high-quality study conduct
Site Activity:
Primary site: London
Expected on-site presence: 2–3 times per month , depending on study needs
Some remote monitoring for sites in Scotland and Ireland
What We’re Looking For:
- Proven Senior CRA experience within medical devices or relevant clinical research
- Strong monitoring and site management skills
- Confident communicator who can drive engagement across multiple sites
- Ability to work independently in a flexible, part-time arrangement
- Available to start January
Why Join?
- Opportunity to work on an exciting vascular device study
- High visibility within an agile, expert team
- Flexible part-time schedule
- Direct interaction with senior leaders and decision-makers
If you’re looking for a part-time contract where you can truly make an impact, we’d love to hear from you. Apply today or get in touch for further details.