A leading clinical research firm is seeking a Senior Regulatory & Start Up Specialist to manage end-to-end site activities for clinical studies based in Mexico. The role involves ensuring site qualification, document collection, and submissions to Ethics Committees and Regulatory Authorities. Candidates should have a Bachelor's degree, three years of relevant experience in the biopharmaceutical industry, and strong English communication skills. This is a full-time position with a focus on innovative medical treatments to enhance patient outcomes.