CRA II / SCRA II Midlands

Meeveem Limited; West Midlands; On-site; GBP 42,000 - 56,000; Full time

Job summary

Fortrea is hiring a CRA II/SCRA to join our UK team, with opportunities across the Midlands. The role focuses on monitoring studies, ensuring regulatory compliance, and maintaining data integrity, while supporting feasibility and recruitment activities.

Ideal candidates have a life sciences degree, 2+ years in a related role, and a valid driving licence with willingness to travel across sites in the Midlands. You will work within a collaborative team, adhering to SOPs and regulatory guidelines.

Qualifications

• Bachelor's/degree in life sciences or allied health field.
• At least 2 years of CRA/Site Management experience.
• Knowledge of Regulatory Guidelines and the clinical trial process.
• Strong communication, organizational, and problem-solving skills.
• Valid driving licence and willingness to travel.

Responsibilities

• Conduct and oversee study site monitoring visits to ensure compliance with protocols and regulatory requirements.
• Manage 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.
• Track and report Serious Adverse Events (SAEs).

Skills

Communication skills

Organizational skills

Problem-solving

Driving licence

Willingness to travel

Education

Life sciences degree

Job description

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.

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.