Site Activation Coordinator

Medpace; Buenos Aires; Presencial; ARS 2.700.000 - 3.200.000; Jornada completa

Descripción de la vacante

Medpace is seeking a Regulatory Submissions Coordinator for our Buenos Aires office to support ethics submissions and regulatory documentation. You will work closely with Regulatory Submissions Coordinators and Start Up teams to help ensure timely delivery of study materials and regulatory compliance.

The role requires 1–3 years of regulatory submissions experience, a Life Sciences background, and strong organizational and communication skills.

Formación

• Bachelor's degree required (Life Sciences preferred) and 1–3 years of regulatory submissions experience.
• Excellent organizational and prioritization skills are essential.
• Knowledge of Microsoft Office.
• Great attention to detail and strong written and verbal communication.
• Fluency in spoken and written English.

Responsabilidades

• 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.
• Perform other tasks as needed.

Conocimientos

Regulatory submissions experience

Organizational skills

English fluency

Communication skills

Educación

Bachelor's degree in Life Sciences

Herramientas

Microsoft Office

Descripción del empleo

Join 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.

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;
• Perform other tasks as needed.

Qualifications

• Bachelor'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; and
• Fluency in spoken and written English.

We kindly ask to submit applications in English.

Medpace Overview

Medpace 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 Work

• Work alongside physicians, scientists, and industry-leading experts committed to advancing the global development of medical therapeutics through clinical research excellence

Collaborative Culture

• Contribute 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 approachable

Continuous Growth & Development

• Office based environment with on-site mentors
• Defined career paths with clear advancement opportunities
• Industry renowned onboarding and training programs designed to accelerate professional development
• Ongoing training and continuous learning opportunities throughout your career
• An environment that encourages employees to influence change, contribute ideas, and grow quickly

Other Employee Benefits

• Competitive compensation programs that recognize and reward performance
• Comprehensive health, wellness, retirement, and PTO benefits
• Office based culture with occasional WFH that provides flexibility for eligible positions after training
• Company-sponsored social events

Please note benefits may vary based on country.

What To Expect Next

A 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.