Clinical Safety Coordinator at Medpace, Inc.

Campinas, São Paulo, Brazil -

Full Time

Start Date

Immediate

Expiry Date

26 Jun, 26

Salary

0.0

Posted On

28 Mar, 26

Experience

2 year(s) or above

Remote Job

Yes

Telecommute

Yes

Sponsor Visa

Skills

Pharmacovigilance, Safety Reporting, Regulatory Timelines, Good Clinical Practice, Medical Terminology, Electronic Data Capture, Clinical Databases, Safety Reporting Guidelines, Attention To Detail, Clinical Operations Interaction, Data Management Interaction, Regulatory Submissions Interaction

Industry

Pharmaceutical Manufacturing

Description

Our Latin American activities are growing rapidly, and we are currently seeking a full-time, office-based Clinical Safety Coordinator to join our team in Sao Paulo! This position plays a key role in the pharmacovigilance process at Medpace. Working in a team to accomplish tasks and projects that are instrumental to the company’s success. If you want an exciting career where you use your previous expertise and can develop and grow your career even further, then this is the opportunity for you. Responsibilities • Oversight of submission of safety reports in the appropriate format to Competent Authorities/Ethics Committees in compliance with regulatory timelines; • Regular interaction with other internal departments globally and locally, such as, Clinical Operations, Data Management and Regulatory Submissions; • Draft study specific safety documents as required. • Work in a global team to distribute safety reports globally Qualifications • Bachelor's degree in Life Science area required; • 2-3 years of experience of working within drug safety preferred; • Demonstrate fundamental knowledge of Good Clinical Practice (GCP) guidelines and medical terminology; • Knowledge of Electronic Data Capture (EDC) systems and other clinical databases; • Experience safety reporting to regulatory authorities in Spanish speaking LATAM countries; • Knowledge of applicable safety reporting guidelines; and • Strong attention to detail; Medpace Overview Medpace is a full-service clinical contract research organization (CRO). We provide Phase I-IV 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 its scientific and disciplined approach. We leverage local regulatory and therapeutic expertise across all major areas including oncology, cardiology, metabolic disease, endocrinology, central nervous system, anti-viral and anti-infective. Headquartered in Cincinnati, Ohio, employing more than 5,000 people across 40+ countries. Why Medpace? People. Purpose. Passion. Make a Difference Tomorrow. Join Us Today. The work we’ve done over the past 30+ years has positively impacted the lives of countless patients and families who face hundreds of diseases across all key therapeutic areas. The work we do today will improve the lives of people living with illness and disease in the future. 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 Awards Recognized by Forbes as one of America's Most Successful Midsize Companies in 2021, 2022, 2023 and 2024 Continually recognized with CRO Leadership Awards from Life Science Leader magazine based on expertise, quality, capabilities, reliability, and compatibility What to Expect Next A Medpace team member will review your qualifications and, if interested, you will be contacted with details for next steps.

Responsibilities

The coordinator will oversee the submission of safety reports to Competent Authorities/Ethics Committees, ensuring compliance with regulatory timelines. This role involves regular interaction with global and local internal departments like Clinical Operations and Data Management, and drafting study-specific safety documents.