Join Medpace as a full‑time, office‑based Regulatory Submissions Manager in Mexico City. This role plays a key part in the study start‑up process, building on your experience in clinical trials and regulatory submissions. You will use your expertise to develop and grow your career while supporting our LATAM clinical trial activities. Responsibilities Efficiently manage and successfully execute all aspects of global start‑up. Perform quality checks on submission documents and site essential documents. Prepare and approve informed consent forms. Review pertinent regulations to develop proactive solutions to start‑up issues and challenges. Present during bid defenses, general capabilities meetings, and audits. Qualifications Submit your CV in English. Minimum education: bachelor’s degree in a life science major. At least 4 years of regulatory submissions/start‑up management experience, leading regulatory/start‑up project teams. Knowledge and experience of Clinica...