Teams at Fortrea

Support regional compensation activities including salary surveys, job evaluations, market pricing, reporting, and global compensation review cycles. Prepare summaries and assist with compensation program delivery while ensuring data accuracy, confidentiality, and compliance.

Prepare, review and negotiate site, confidentiality, and other clinical trial contracts; track and document contract status; ensure SOP and ICH-GCP compliance; coordinate with clinical, legal and project teams; identify and escalate contracting risks; provide regular status updates to support study timelines.

Monitors and manages clinical trial sites from startup through closeout, conducting site visits, training teams, reviewing source data, ensuring protocol and ICH-GCP compliance, supporting audit readiness, and resolving site-level issues. Collaborates with sponsors, vendors, and cross-functional teams while traveling to investigator sites as needed. Requires clinical monitoring experience, relevant education, strong communication skills, language fluency, and a valid driver’s license.