Teams at Fortrea

Lead product strategy and development for data management solutions in life sciences, ensuring market relevance and user satisfaction while managing lifecycle and stakeholder alignment.

Independently monitor clinical trial sites per SOPs, ICH GCP and sponsor requirements: perform initiation, routine, and close-out visits; verify informed consent, source data, eCRF review, and IP accountability; manage regulatory/ eTMF documents, SAE follow-up, trip reports, and site training. Support project plans, ensure audit readiness, and maintain study timelines while traveling to sites (60%).

Support clinical project execution and site monitoring under SOPs, ICH and GCP. Conduct remote and onsite visits, source data verification, CRF review, reporting, site initiation/close-out, drug accountability, safety follow-up, and study administration while completing Fortrea MEA training.