Jobs at Fortrea

Conducts clinical trial site management and monitoring, including initiation, routine, process, and close-out visits. Ensures informed consent, protocol, regulatory, data integrity, investigational product, and audit-readiness requirements are met. Performs source document verification, eCRF review, query resolution, SAE follow-up, regulatory document maintenance, site training, and monitoring-plan execution. Collaborates with study teams, prepares reports, manages trial systems, and travels approximately 60% to study sites.

Conducts clinical trial site monitoring and management, including initiation, routine monitoring, closeout, source-data verification, regulatory compliance, SAE follow-up, CRF review, query resolution, audit readiness, and investigator coordination. Leads limited-scope projects, supports protocol and report development, manages vendors and study supplies, assists with budgets and regulatory submissions, and mentors junior staff. The role requires extensive overnight travel, strong clinical research and site-management expertise, and at least three years of clinical monitoring experience.

Leads business development and Account Executive teams across South Korea, India, Australia, New Zealand, Thailand, and Taiwan. Responsibilities include territory planning, sales forecasting, account development, client relationship management, pricing negotiations, team hiring and coaching, pipeline management in Salesforce, market intelligence, strategic partnerships, and executive reporting. Requires extensive pharmaceutical and biotechnology services sales experience, global collaboration, leadership, negotiation, and frequent international travel.