CRA II North West

Maidenhead - UK

Monthly Salary: Not Disclosed

Posted on: Yesterday

Vacancies: 1 Vacancy

Job Summary

Are you looking to grow your career in clinical research

Fortrea is hiring a CRAII to join our client-dedicated team. This role is based in the North West offering an exciting opportunity to work on diverse studies while ensuring compliance with regulatory guidelines and company SOPs.

Why Join Fortrea

Be part of a global innovative organization driving advancements in clinical research.
Work on cutting-edge trials across a range of therapeutic areas.
Enjoy flexible career progression with opportunities at different CRA levels.
Benefit from a collaborative team environment that values mentorship and growth.

Key Responsibilities

Conduct and oversee study site monitoring visits to ensure compliance with protocols and regulatory requirements.
Manage all aspects of site activities including site initiation monitoring visits and closeouts.
Ensure patient safety data integrity and adherence to GCP guidelines.
Support feasibility assessments investigator recruitment and vendor coordination.
Mentor junior team members and contribute to quality control efforts.
Track and report Serious Adverse Events (SAEs) as required.

Qualifications

Bachelors or Masters degree in Life Sciences or equivalent.
3 years of relevant clinical research experience with at least 1 year of previous monitoring experience.
Ability to work independently and manage multiple priorities.
Basic knowledge of regulatory guidelines and the clinical trial process.
Strong communication organizational and problem-solving skills.
Valid drivers license and willingness to travel nationally (68 visits/month).

Ready to take the next step in your CRA career
Apply now and be part of groundbreaking clinical research at Fortrea!

Learn more about our EEO & Accommodations request here.

Are you looking to grow your career in clinical researchFortrea is hiring a CRAII to join our client-dedicated team. This role is based in the North West offering an exciting opportunity to work on diverse studies while ensuring compliance with regulatory guidelines and company SOPs.Why Join Fortrea...