Clinical Research Associate - Oncology

ICON; Long Beach (CA); Remote; USD 80,000 - 120,000; Full time

Job summary

ICON is seeking an experienced CRA with a strong background in Oncology to join our team in a dynamic and innovative environment. This role offers the chance to partner with a leading global pharmaceutical company, contributing to key monitoring activities and enhancing site performance. Ideal candidates will be adept at managing study sites and training staff while maintaining high standards of data integrity.

Qualifications

• Strong experience in Oncology and clinical research monitoring required.

Responsibilities

• Select potential investigators and provide monitoring visit reports.
• Drive study performance and escalate issues as needed.
• Train site staff in study-related matters.

Skills

Oncology experience

Clinical research monitoring

Data verification

Performance management

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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