Marin Lolić is a dedicated pharmacovigilance and drug safety professional with extensive experience in regulatory submissions, adverse event management, and compliance within both clinical trials and post-market surveillance. Skilled in working with leading safety databases such as Argus, Veeva Vault, and Safety Easy, he has successfully managed individual case safety reports (ICSRs), periodic safety updates, and gateway-to-gateway submissions to global health authorities.

Throughout his career, Marin has held roles ranging from PV Associate to Team Leader and Global Drug Safety Specialist, demonstrating both technical expertise and strong leadership capabilities. His achievements include coordinating international safety management plans, leading data migration projects, and ensuring continuous adherence to global regulatory requirements. He is also recognized for fostering collaboration across cross-functional teams and building efficient safety workflows.

Holding degrees in Biology and Chemistry, Drug Research and Development, and Management, Marin combines a scientific foundation with strategic oversight. Fluent in English and experienced in multinational environments, he brings a unique mix of technical proficiency, regulatory knowledge, and leadership skills to every project.