Clinical Trials Admin & TMF Specialist

ICON in Mexico City is seeking a SMA II to facilitate clinical trials by ensuring compliance with protocols and GCP guidelines. The role involves managing Trial Master File documentation and supporting site activation. Candidates should have a Bachelor's degree in life sciences and at least 2 years of clinical research experience. This position is office-based for the first 6 months and then transitions to a hybrid work model. ICON offers competitive salary and benefits focused on work-life balance.