Experienced CRAs

Fortrea; Remote; GBP 60,000 - 80,000; Full time

Job summary

A leading clinical research organization is looking for experienced Clinical Research Associates (CRAs) with a minimum of 2 years independent monitoring experience. This remote role allows you to work on diverse studies while ensuring compliance with regulatory guidelines. Candidates should have a Life Sciences degree, relevant clinical research experience, and strong communication skills. You will conduct monitoring visits, manage site activities, and support junior team members. Join a team that values mentorship and offers flexible career progression.

Benefits

Flexible career progression

Collaborative team environment

Mentorship opportunities

Qualifications

• ≥ 3 years of relevant clinical research experience.
• At least 2 years of previous monitoring experience.
• Ability to work independently and manage multiple priorities.

Responsibilities

• Conduct study site monitoring visits to ensure compliance.
• Manage site activities, including initiation and closeouts.
• Ensure patient safety and data integrity.

Skills

Independent monitoring

Regulatory compliance

Communication

Problem-solving

Organizational skills

Education

Bachelor’s or Master’s degree in Life Sciences

Job description

Are you looking to grow your career in clinical research?

Fortrea is hiring experienced CRAs (minimum of 2 years of independent monitoring experience) on different levels of seniority to join our client‑dedicated team. This role is remote, 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

• Bachelor’s or Master’s degree in Life Sciences or equivalent.
• ≥ 3 years of relevant clinical research experience, with at least 2 years 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 driver’s license and willingness to travel nationally (6-8 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.