CRA II Midlands

Fortrea; Maidenhead; On-site; GBP 30,000 - 60,000; Full time

Job summary

An innovative global organization is seeking Clinical Research Associates (CRAs) at various seniority levels to join their dynamic team. This role offers a unique opportunity to work on cutting-edge clinical trials across diverse therapeutic areas while ensuring compliance with regulatory guidelines and company SOPs. You'll conduct site monitoring visits, manage site activities, and mentor junior team members in a collaborative environment that values growth and mentorship. If you're ready to advance your career in clinical research and make a significant impact, this is the perfect opportunity for you!

Benefits

Flexible Career Progression

Collaborative Team Environment

Mentorship Opportunities

Qualifications

• University degree in life sciences or allied health field required.
• 1+ year experience in Site Management or CRA role preferred.

Responsibilities

• Conduct study site monitoring visits for compliance.
• Manage site activities including initiation and closeouts.
• Mentor junior team members and ensure patient safety.

Skills

Communication Skills

Organizational Skills

Problem-Solving Skills

Knowledge of Regulatory Guidelines

Clinical Trial Process Knowledge

Education

Degree in Life Sciences

Relevant Allied Health Field Degree

Tools

GCP Guidelines

Job description

Are you looking to grow your career in clinical research? Fortrea is hiring CRAs at various seniority levels to join our dynamic team. We have opportunities based in London and 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 1 year 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.

Ready to take the next step in your CRA career? Apply now and be part of groundbreaking clinical research at Fortrea!