Job SummaryJoin Medpace in our Buenos Aires office!
As a Regulatory Submissions Coordinator you will have the opportunity to work within Regulatory Submissions, supporting our many projects and gaining some vital experience.
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.ResponsibilitiesProvide 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;Perform other tasks as needed.QualificationsBachelor's degree is required (preferably in a Life Sciences field) and at least 1-3 years of regulatory submissions experience;Excellent organizational and prioritization skills;Knowledge of Microsoft Office;Great attention to detail and excellent oral and written communication skills; andFluency in spoken and written English.We kindly ask to submit applications in English.Medpace OverviewMedpace is a full-service clinical contract research organization (CRO) providing phase l-lV clinical development services to the biotechnology, pharmaceutical, and medical device industries.
Our mission is to accelerate the global development of safe and effective medical therapeutics through the advancement of clinical research.
We leverage in-country regulatory and therapeutic expertise across all major therapeutic areas including oncology, cardiology, metabolic, endocrinology, central nervous system,



and anti-viral and anti-infective.
Headquartered in Cincinnati, Ohio, we employ more than 6,500 people across 40+ countries.Why Medpace?
When you join Medpace, you become part of an innovative team that brings cutting-edge therapies to market while building a meaningful and rewarding career focused on scientific excellence and improving patient outcomes around the world through continuous learning and cross-functional collaboration.Purpose-Driven WorkWork alongside physicians, scientists, and industry-leading experts committed to advancing the general development of medical therapeutics through clinical research excellenceCollaborative CultureContribute to an interactive team environment that empowers decision making, creative thinking, and continuous learning through open communication and mutual trust.Leadership throughout Medpace is both accessible and approachableContinuous Growth & DevelopmentOffice based environment with on-site mentorsDefined career paths with clear advancement opportunitiesIndustry renowned onboarding and training programs designed to accelerate professional developmentOngoing training and continuous learning opportunities throughout your careerAn environment that encourages employees to influence change, contribute ideas, and grow quicklyOther Employee BenefitsCompetitive compensation programs that recognize and reward performanceComprehensive health, wellness, retirement, and PTO benefitsOffice based culture with occasional WFH that provides flexibility for eligible positions after trainingCompany-sponsored social eventsPlease note benefits may vary based on country.What to Expect NextA Medpace team member will review your application and if your profile matches our current needs, you will be contacted for an interview.
While we review all applications carefully, we are unable to respond to every applicant, and only candidates selected for interviews will be contacted.
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📌 Site Activation Coordinator (Buenos Aires)
🏢 Medpace
📍 Buenos Aires