Experienced CRAs

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

• Bachelors or Masters 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 drivers license and willingness to travel nationally (68 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.