CRA II - SCRA II - Midlands - FSP

Fortrea; Maidenhead; On-site; GBP 35,000 - 54,000; Full time

Job summary

Fortrea is hiring a CRA II/SCRA to join our fast-growing FSP team across the UK. You will monitor sites, ensure compliance with protocols, regulatory requirements and GCP guidelines, and support diverse therapeutic studies.

We value mentorship and growth, offering flexible career progression and opportunities at different CRA levels. A valid driver's license and willingness to travel are essential as travel across sites is expected.

Qualifications

• University/college degree in life sciences or allied health field.
• At least 2 years of site management/CRA experience.
• Knowledge of regulatory guidelines and GCP.
• Strong communication, organisation, and problem-solving skills.
• Valid driver's license and willingness to travel.

Responsibilities

• Conduct and oversee study site monitoring visits to ensure protocol compliance.
• Manage site activities from initiation to closeout.
• Ensure patient safety, data integrity, and GCP adherence.
• Support feasibility assessments, investigator recruitment, and vendor coordination.
• Mentor junior team members and track/report SAEs.

Skills

Regulatory guidelines knowledge

Strong communication

Willingness to travel

Driver's license

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 .