Regulatory Affairs Sr. Associate — IIP Lead (Hybrid)

A leading pharmaceutical company in Colombia is seeking an Investigator Initiation Package Sr. Associate to ensure regulatory compliance and support projects in drug development. The role involves managing timelines, performing QC checks, and delivering on clinical study portfolios. Candidates should have a Bachelor's degree and 3+ years of experience in electronic submissions within the pharmaceutical industry. This position is hybrid and requires strong attention to detail and organizational skills. #J-18808-Ljbffr