CRA II Midlands

Are you looking to grow your career in clinical research? Fortrea is hiringCRAs at various seniority levelsto join our dynamic team. We have opportunities based inLondon 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 aglobal, innovative organizationdriving advancements in clinical research.
• Work on cutting-edge trials across a range of therapeutic areas.
• Enjoyflexible career progression, with opportunities at different CRA levels.
• Benefit from acollaborative team environmentthat 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, includingsite initiation, monitoring visits and closeouts.
• Ensure patient safety, data integrity, and adherence toGCPguidelines.
• Support feasibility assessments, investigator recruitment and vendor coordination.
• Mentor junior team members and contribute to quality control efforts.
• Track and reportSerious Adverse Events (SAEs)as required.
  

Qualifications:

• University/college degree in life sciences or a relevant allied health field.
• At least1 yearof experiencein a related role (e.g., Site Management, CRA).
• Basic knowledge ofRegulatory Guidelines and the clinical trial process.
• Strong communication, organizational, and problem-solving skills.
• Avalid driver’s licenseand willingness to travel.
  

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

Learn more about ourEEO & Accommodations request here.