Clinical Research Associate - Oncology

ICON plc; United Kingdom; On-site; GBP 40,000 - 55,000; Full time

Job summary

A leading clinical research organization is seeking an experienced CRA with oncology background to join their team. The successful candidate will contribute to a dynamic environment focused on clinical excellence and innovation, working with major pharmaceutical partners to drive study success and patient outcomes.

Qualifications

• Strong experience in oncology and clinical research monitoring.
• Right-to-work status in the UK.
• Ability to proactively identify and resolve study-related issues.

Responsibilities

• Contribute to the selection of potential investigators.
• Provide monitoring visit reports within timelines.
• Drive performance at study sites and train site staff.

Skills

Oncology experience

Clinical research monitoring

Data query resolution

Investigator training

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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