IntroductionTFS 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 ResponsibilitiesAs 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 and 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 OfferTFS 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 ApplyIf 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.

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