Our LATAM clinical trial activities are growing rapidly, and we are currently seeking a full-time, Office‑Based Regulatory Submissions Manager to join our Study Start‑Up team in Buenos Aires! This position plays a key role in the study start‑up process at Medpace.

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.
• At least 4 years of regulatory submissions/start‑up management experience (leading regulatory/start‑up project teams).
• Knowledge and experience of Clinical Trial Applications...