Job Summary Join Medpace at our Mexico City offfice! As a Regulatory Submissions Coordinator you will have the opportunity to work within Regulatory Submissions, supporting our many projects and gaining vital experience in study start up! You will be a productive member of the team, and will be mentored and supported as you develop your skills. Working directly with Regulatory Submissions Coordinators, you will gain valuable hands on experience to enable you to develop a career in clinical research. Responsibilities Provide day-to-day departmental/project support activities, such as collection of vital documents for ethics submissions and preparation of study documents to competent authorities; Support Regulatory Submission Managers and Start Up teams in ensuring deadlines are adhered to; Conduct quality control of documents; Provide advice and guidance to internal and external team members to ensure compliance with applicable regulations and requirements; and Perform other tasks as needed. Qualifications Bachelor's degree is required (preferably in a Life Sciences field) 1-3 years of regulatory submissions / study start up experience preferred; Ability to work in office; Excellent organizational and prioritization skills; Knowledge of Microsoft Office; Great attention to detail and excellent oral and written communication skills; and Fluency in spoken and written English. Medpace Perks Flexible work environment Competitive compensation and benefits package Competitive PTO packages Structured career paths with opportunities for professional growth Company-sponsored employee appreciation events Employee health and wellness initiatives #J-18808-Ljbffr