Description
ICON is hiring a Study Start Up Associate II to lead the initiation of clinical trials in Brazil or Mexico. The role covers regulatory document preparation and submission, coordination with internal and external stakeholders, recordkeeping, guidance to study teams, and process improvement. Candidates need a bachelor's degree in life sciences or a related field, at least two years of clinical research or regulatory affairs experience, knowledge of ICH-GCP and local regulatory requirements, strong organizational and communication skills, and willingness to travel approximately 5%. The position is remote and offers medical, dental, and vision coverage where applicable, along with retirement, life assurance, disability, and learning benefits.
