Recibir nuevas ofertas de empleo por email
- ...advisor on clinical trials across multiple regions. The role involves providing scientific expertise, medical protocol reviews, adverse event assessment, and clinical support throughout the trial lifecycle. Responsibilities Serve as global medical advisor on assigned...
- ...monitoring across global clinical trials; serve as Medical Monitor and primary medical interface Review protocols, safety data, adverse events, and critical clinical findings; ensure GCP compliance and timely safety reporting Train study teams and investigators on...
- ...requiring site investigation Evaluate inclusion/exclusion criteria compliance and protocol adherence across dosing and adverse events Assess laboratory results, concomitant medications, and medical history completeness Verify end-of-treatment and end-of-study...