Work Schedule Standard (Mon-Fri) Environmental Conditions Office Provides medical oversight of clinical trials to ensure company SOPs, client directives, good clinical practice, and regulatory requirements are followed. Attends and presents at investigator and sponsor meetings, provides
Education and Experience : - Suitable clinical trial experience in a Contract Research Organization, pharmaceutical company or as a principal investigator (comparable to 1-2 years) in the industry; Or - Direct experience in safety/Pharmacovigilance (comparable to 2
Work ScheduleStandard (Mon-Fri) Environmental ConditionsOffice Job Description Join us as a Medical Director M-SERM - And lead our efforts in medical safety evaluation and risk management. What You’ll Do: • Maintain understanding of methods for recording
Pharmacovigilance (Associate & Senior Assocaite) - BRAZIL ICON plc is a world-leading healthcare intelligence and clinical research organization. We’re proud to foster an inclusive environment driving innovation and excellence, and we welcome you to join us