Clinical Research Associate - Oncology

ICON Strategic Solutions; United Kingdom; Remote; GBP 45,000 - 65,000; Full time

Job summary

Une entreprise de recherche clinique dynamique recherche un CRA basé au Royaume-Uni pour rejoindre une équipe dédiée à l'oncologie. Vous aurez l’occasion de travailler avec une grande entreprise pharmaceutique, dans un environnement innovant où votre contribution peut jouer un rôle clé dans l'amélioration des soins aux patients. Ce poste est destiné aux candidats possédant une expérience solide en oncologie et une approche proactive de la gestion des études cliniques.

Qualifications

• Expérience solide en oncologie dans un cadre de recherche clinique.
• Droit de travail au Royaume-Uni requis.
• Capacité à identifier et résoudre les problèmes liés à l'étude.

Responsibilities

• Contribuer à la sélection des investigateurs.
• Fournir les rapports de visite de surveillance dans les délais requis.
• Former et soutenir le personnel d'étude dans les questions liées à l'étude.

Skills

Oncology experience

Clinical research monitoring

Performance management

Data verification

Job description

Experienced, high-performing, UK-based CRA/clinical research associate required to augment existing Oncology CRA team, for pharmaceutical and biotechnology company company partner.

You will be partnering with a well-known global pharmaceutical company with a strong portfolio in cardiovascular, gastrointestinal, infection, neuroscience, respiratory and inflammation medicines.

You will have an opportunity to work in a solid partnership and an environment driven by innovation and continuous improvement. This program is for you if you are looking for an environment where people feel they belong and are empowered to reach their full potential, perform at their best and make a valued contribution to saving lives.

Amongst other tasks, your main responsibilities will be to;

• Contribute to the selection of potential investigators.
• Provide the required monitoring visit reports within required timelines
• Drive performance at the sites. Proactively identify study-related issues and escalate as appropriate.
• Perform source data verification according to SDV plan and ensure data query resolution
• Initiate, monitor and close study sites in compliance with client Procedural Documents. Share information on patient recruitment and study site progress within local Study Delivery Team.
• Train, support and advise Investigators and site staff in study related matters.

We are looking for candidates with strong Oncology experience working in a clinical research monitoring capacity, and residing in Northern England or Midlands, UK (with appropriate right-to-work in the UK already granted, if applicable)

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