Company DescriptionJob DescriptionPurpose Statement:Collaborate with the coordination of planning, implementation, and conduction of local and general clinical studies (Post-Marketing Observational, Multi-Country Non-Interventional, Investigator Initiated, Non-AbbVie Sponsored Collaborative and Pharmacoeconomic) and Pre-Approval Access programs (PAAs) according to
CDMXWhat You Will DoTrial Documentation & eTMF ManagementOversee clinical trial documentation, including CTA packages for Health Authority (HA) and Ethics Committee (EC) submissions.Maintain and ensure compliance of the electronic Trial Master File (eTMF), including timely uploads, quality
About Oliver WymanAt Oliver Wyman, a Marsh (NYSE: MRSH) business, we bring deep industry insight, bold innovation, and a collaborative approach that cuts through complexity to help organizations navigate their most defining transformative moments. As a