Join the world's largest & most comprehensive clinical research organisation, powered by healthcare intelligence, as a CRA. […]
Serve as the primary contact between the sponsor and investigational sites.
Ensure trial sites are inspection-ready by complying with the clinical research protocol, company's SOPs, GCP, and applicable regulations from start-up to database lock.
Manage site selection, pre-trial assessments, subject recruitment and retention, site initiation, monitoring, and close-out.
Collaborate with the CTA, LTM, and GTM to oversee site management and perform trial-related activities...