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Clinical Research Associate - Biopharma

Pharmaceutical Research Associates, Inc

United Kingdom

On-site

GBP 60,000 - 80,000

Full time

16 days ago

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An established industry player seeks a Biopharma Regional CRA to join their innovative team. This role offers the chance to collaborate with a renowned global pharmaceutical company, focusing on impactful therapeutic areas such as cardiovascular and neuroscience. You will thrive in a supportive environment where your contributions are valued, and you can truly make a difference in patients' lives. If you possess strong clinical research monitoring skills and reside in Northern England or Scotland, this opportunity is perfect for you to advance your career while being part of a mission-driven organization.

Strong experience in clinical research monitoring is essential.
Candidates must reside in Scotland or Northern England.

Contribute to investigator selection and monitor study sites.
Drive site performance and resolve study-related issues.

Clinical Research Monitoring

Data Verification

Performance Management

Training and Support

Overview

Experience Biopharma Regional CRA/clinical research associate (ideally residing in Northern England/Scotland) required for Global Pharmaceutical company.

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.

Responsibilities

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.

Qualifications

Strong experience working in a clinical research monitoring capacity, and residing in Scotland/North UK (with appropriate right-to-work in the UK already granted, if applicable).

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