Senior Clinical Research Associate

TFS HealthScience; London; On-site; GBP 100,000 - 125,000; Part time

Job summary

A leading global Contract Research Organization is seeking a Senior CRA based in the UK to oversee compliance and monitoring activities for clinical trials in London. The successful candidate will have a minimum of 3 years of independent monitoring experience, a relevant degree, and ISO 14155 certification. This part-time role offers a competitive compensation package and a focus on work-life balance within a supportive environment.

Benefits

Competitive compensation package

Flexible contract structure

Supportive work environment

Qualifications

• Current certification in ISO 14155 for medical device clinical investigations.
• Minimum of 3 years of independent, on-site monitoring experience as a CRA.
• Experience supporting clinical trials within the medical device sector is preferred.

Responsibilities

• Conduct monitoring activities in adherence to regulatory standards.
• Ensure protection of study participants and verify informed consent.
• Manage site relationships and provide ongoing support to site staff.

Skills

Independent on-site monitoring

Communication skills

Problem-solving skills

Organizational skills

Education

Bachelor’s degree or higher in Life Sciences, Nursing, or a related field

Tools

ISO 14155 certification

Job description

Introduction

TFS HealthScience is a leading global mid-size Contract Research Organization (CRO) that partners with biotechnology and pharmaceutical companies to deliver transformative clinical development programs. We combine the full-service capability and resourcing solutions of a large CRO with the agility and personalized partnership of a mid-size provider.

Key Responsibilities

As a Senior CRA, you will be the primary point of contact for a designated clinical site, ensuring compliance and excellence throughout the trial lifecycle. Your duties will include:

• Conducting all monitoring activities (site initiation, routine monitoring, and close-out visits) in strict adherence to ISO 14155, ICH-GCP, and other applicable regulatory standards.
• Ensuring the protection of study participants by verifying proper informed consent procedures and upholding the highest standards of subject safety.
• Guaranteeing protocol compliance and data integrity through meticulous review of source documents and accurate transcription to Case Report Forms (CRFs).
• Managing site relationships effectively, providing ongoing support and training to site staff to ensure smooth study conduct.
• Proactively identifying and resolving site issues, with comprehensive documentation and timely escalation as necessary.

Qualifications & Experience

• Essential: Current certification in ISO 14155 for medical device clinical investigations.
• Bachelor’s degree or higher in Life Sciences, Nursing, or a related field.
• A minimum of 3 years of independent, on-site monitoring experience as a CRA.
• Proven experience supporting clinical trials within the medical device sector is strongly preferred.
• Demonstrated ability to work autonomously, manage a decentralized workload, and excel in a home-based environment.
• Exceptional organizational, communication, and problem-solving skills.
• Must be based in the UK and available for regular travel to a single site in London. Proximity to London is a significant advantage.

What We Offer

TFS HealthScience is committed to investing in our talent. By joining our team, you will receive:

• A competitive, pro-rated compensation package with a flexible contract structure.
• The opportunity to contribute to a high-profile study at a world-class academic institution.
• A supportive and innovative environment within a global CRO that values expertise and work-life balance.
• A focused role with a manageable travel schedule to a single site.

How to Apply

If you are a certified, UK-based CRA with medical device experience looking for a engaging part-time opportunity, we encourage you to apply by submitting your CV and a cover letter.