CRA II - SCRA II - Midlands - FSP

FTMAI Fortrea Development Ltd; Maidenhead; On-site; GBP 38,000 - 48,000; Full time

Job summary

Fortrea is hiring a CRA II/SCRA to join our dynamic FSP team with opportunities across the UK, particularly in the Midlands. The role focuses on site monitoring, regulatory compliance, and patient safety within diverse therapeutic studies.

Ideal candidates hold a life sciences degree with at least 2 years in a related role, possess strong communication and problem-solving skills, and have a valid driver’s license with willingness to travel.

Qualifications

• University/college degree in life sciences or a relevant allied health field.
• At least 2 years of experience in a related role (e.g., Site Management, CRA).
• Basic knowledge of Regulatory Guidelines and the clinical trial process.
• Strong communication, organizational, and problem-solving skills.
• A valid driver’s license and willingness to travel.

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.

Skills

Site monitoring

GCP

Regulatory knowledge

Communication

Education

Life sciences degree

Job description

Are you looking to grow your career in clinical research? Fortrea is hiring a CRA II/SCRA to join our dynamic FSP team. We have opportunities across the UK, particularly in the Midlands, offering an exciting chance 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

• University/college degree in life sciences or a relevant allied health field.
• At least 2 years of experience in a related role (e.g., Site Management, CRA).
• Basic knowledge of Regulatory Guidelines and the clinical trial process.
• Strong communication, organizational, and problem-solving skills.
• A valid driver’s license and willingness to travel.

Learn more about our EEO & Accommodations request here.

At Fortrea, we're all about turning the “impossible” into "I'm possible." Together, we break barriers to deliver exceptional service to our patients, fueled by a shared commitment to teamwork and excellence. Regardless of your role, we're all family, working together to achieve extraordinary results. At Fortrea, your career isn't just a job – it's a journey of making the exceptional possible, every day.