Clinical Research Associate - Biopharma

ICON; United Kingdom; Remote; GBP 35,000 - 55,000; Full time

Job summary

An established industry player is seeking a Biopharma Regional CRA/Clinical Research Associate to join their innovative team. This role is perfect for those residing in Northern England or Scotland who are passionate about contributing to life-saving initiatives. You will work in a collaborative environment, focusing on clinical research monitoring and site performance management. The company is dedicated to inclusion and belonging, ensuring a workplace free from discrimination. If you have strong experience in clinical research and a desire to make a difference, this opportunity is for you.

Qualifications

• Strong experience in clinical research monitoring required.
• Right-to-work in the UK and residence in Scotland or Northern UK.

Responsibilities

• Contribute to the selection of potential investigators.
• Drive site performance and resolve data queries.
• Train and support investigators on study-related matters.

Skills

Clinical Research Monitoring

Data Verification

Site Performance Management

Investigator Training

Job description

Experience Biopharma Regional CRA/Clinical Research Associate

We are seeking an experienced Biopharma Regional CRA/Clinical Research Associate, ideally residing in Northern England or Scotland, for a global pharmaceutical company.

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

This role offers an opportunity to work in a collaborative environment driven by innovation and continuous improvement. It is suitable for individuals seeking a workplace where they feel a sense of belonging, are empowered to reach their full potential, and can contribute to life-saving initiatives.

Main Responsibilities

1. Contribute to the selection of potential investigators.
2. Provide monitoring visit reports within required timelines.
3. Drive site performance, proactively identify issues, and escalate as appropriate.
4. Perform source data verification according to SDV plan and ensure data query resolution.
5. Initiate, monitor, and close study sites in compliance with procedural documents. Share information on patient recruitment and site progress with the local Study Delivery Team.
6. Train, support, and advise investigators and site staff on study-related matters.

Strong experience in clinical research monitoring is required, along with residence in Scotland or North UK and appropriate right-to-work in the UK.

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Our Commitment

At ICON, inclusion and belonging are core to our culture. We are dedicated to creating an inclusive and accessible environment for all candidates. We are committed to providing a workplace free of discrimination and harassment. All qualified applicants will receive equal consideration for employment regardless of race, color, religion, sex, sexual orientation, gender identity, national origin, disability, or veteran status.