CRA II, client-dedicated

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.