Clinical Research Associate

Entia; London; Hybrid; GBP 100,000 - 125,000; Full time

Job summary

Entia, innovateur en biomédecine, recrute un Clinical Research Associate pour un contrat fixe de 4 mois. Ce rôle essentiel implique la gestion des essais cliniques, l'assurance qualité des données et la collaboration avec les sites NHS. Rejoignez une équipe dynamique pour faire avancer des technologies innovantes de diagnostic in-vitro qui transforment les soins du cancer.

Benefits

Environnement d'équipe collaboratif et soutenant

Expérience au sein d'une entreprise MedTech en pleine croissance

Rémunération compétitive

Qualifications

• Expérience avérée en tant que Clinical Research Associate.
• Connaissance approfondie des processus d'essai clinique et des directives GCP.
• Expérience démontrable dans la gestion des relations avec les sites NHS.

Responsibilities

• Développer et maintenir des relations avec les sites d'essai clinique NHS.
• Assurer le respect des protocoles d'étude et des exigences réglementaires.
• Surveiller la collectivité des données et résoudre les problèmes rencontrés.

Skills

Gestion de site

Assurance qualité des données

Compétences en communication

Détail et organisation

Education

Diplôme en sciences de la vie ou expérience équivalente

Job description

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.

About You:

• 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.

What We Offer:

• 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.

If you are a proactive and dedicated CRA looking for an impactful short-term contract, we encourage you to apply!