Enable job alerts via email!

Clinical Research Associate - Oncology

ICON plc

United Kingdom

On-site

GBP 60,000 - 80,000

Full time

30+ days ago

Boost your interview chances

Create a job specific, tailored resume for higher success rate.

An established industry player is seeking an experienced Clinical Research Associate (CRA) to join their Oncology team. This role offers a unique opportunity to partner with a renowned global pharmaceutical company, where you will contribute to life-saving studies in a collaborative and innovative environment. As a CRA, you will be pivotal in selecting investigators, monitoring study sites, and ensuring data integrity. If you thrive in a setting that values empowerment and continuous improvement, this position is perfect for you. Join a team dedicated to making a difference in the field of healthcare and advancing medical research.

Strong Oncology experience in clinical research monitoring.
Proven ability to drive performance and resolve study-related issues.

Contribute to the selection of potential investigators and monitor study sites.
Perform source data verification and ensure compliance with client documents.

Oncology experience

Clinical research monitoring

Data verification

Investigator training

Degree in Life Sciences

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

Get your free, confidential resume review.

or drag and drop a PDF, DOC, DOCX, ODT, or PAGES file up to 5MB.