CRA II, London (client-dedicated)

FTMAI Fortrea Development Ltd; Maidenhead; On-site; GBP 42,000 - 54,000; Full time

Job summary

Fortrea is hiring a CRA II to join our dynamic FSP team. We have opportunities across the UK, particularly in London for CRAs with Phase I patient-study experience, offering an exciting chance to work on diverse studies while ensuring compliance with regulatory guidelines and company SOPs.

Join a global, innovative organization driving trials across therapeutic areas, with flexible progression and mentorship. Travel within the UK is required to support site monitoring and regulatory compliance.

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).
• Phase I patient-study experience.
• 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

Regulatory knowledge

GCP familiarity

Communication skills

Travel readiness

Education

Degree in life sciences

Job description

Fortrea is hiring a CRA II to join our dynamic FSP team. We have opportunities across the UK, particularly in London for CRAs with Phase I patient-study experience, 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).
• Phase I patient-study experience.
• 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.

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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.