Clinical Research Associate (Fixed-Term Contract: 4 Months)

Entia

Full time, Remote (UK-based with occasional travel to sites and office)

About Entia:

Entia is an at-home blood monitoring company focused on preventing high-cost and life-threatening complications associated with cancer therapy. We've developed the world's first blood analyser to enable cancer patients to self-test in the home which has been commercialised with the likes of Pfizer, the NHS and UK private healthcare providers. As an organisation we are committed to building a world where cancer care is affordable, accessible and delivers quality time for people globally.

The Opportunity:

We are seeking a highly motivated and experienced Clinical Research Associate (CRA) for a 3-4 month fixed-term contract and starting immediately. In this pivotal role, you will be instrumental in the successful delivery of our clinical trials for a groundbreaking in-vitro diagnostic device across multiple centres within the UK. This is an exciting opportunity to contribute to cutting-edge research and make a tangible impact on cancer care.

Key Responsibilities:

• Site management: Develop and maintain strong, collaborative relationships with NHS clinical trial sites across the UK, acting as the primary point of contact for all study-related activities.
• Trial oversight: Ensure the smooth and efficient progression of clinical trials, adhering to study protocols, Good Clinical Practice (GCP) guidelines, and all applicable regulatory requirements.
• Data quality assurance: Oversee and assure the quality of data collection at sites, including source data verification, query resolution, and accurate completion of Case Report Forms (CRFs).
• Site monitoring & audits: Conduct regular site visits (remote and on-site as required) to monitor study progress, provide training, review essential documents, and perform site audits to ensure compliance and data integrity.
• Problem solving: Proactively identify and resolve issues or challenges that may arise during the course of the clinical trial, escalating as appropriate.
• Documentation and reporting: Contribute to the preparation and review of study files, clinical study reports, maintenance of ethics approvals, and other essential documentation.
• Training & support: Provide ongoing training and support to site staff on study protocols, procedures, and data entry requirements.

• Proven experience as a Clinical Research Associate and with experience in IVD or medical device trials.
• In-depth knowledge of clinical trial processes and GCP guidelines.
• Demonstrable experience in managing relationships with NHS sites.
• Excellent attention to detail and strong organizational skills.
• Proficient in data review and query resolution.
• Strong communication and interpersonal skills, with the ability to build rapport with diverse stakeholders.
• Ability to work independently and as part of a dynamic team.
• Willingness to travel frequently across the UK to clinical trial sites.
• A relevant life science degree or equivalent experience.

• The opportunity to work on an innovative IVD technology that will make a real difference to cancer patients lives.
• A collaborative and supportive team environment.
• The chance to gain valuable experience within a fast-growing MedTech company at the forefront of cancer care.
• Competitive remuneration for the contract duration.