Clinical Research Associate

Responsibilities

• Conduct pre-study, initiation, monitoring, and closeout visits for research sites according to Medpace/Sponsor SOPs and GCP
• Maintain ongoing site correspondence and site files
• Complete visit reports and maintain study-related databases
• Provide oversight and interaction with clinical research sites
• Review patient charts and clinical research data

Requirements

• Bachelor’s degree in science from an accredited university
• At least 1 year of experience as a Clinical Research Associate (CRA) or Clinical Research Coordinator (CRC)
• Bilingual proficiency in both English and French (written and verbal)
• Thorough knowledge of ICH E-6 guidelines and Health Canada Food and Drug regulations (Part-C, Division 5)
• Ability to travel between 60-80%
• Strong attention to detail, organization, and ability to prioritize workloads across multiple studies
• Proficiency in Microsoft Office

Benefits

• Competitive bonus plans including Resourcing Bonuses and Yearly Travel Incentives
• Home office furniture allowance, mobile phone, and internet hotspot
• Customized PACE training program for expedited onboarding
• Flexible work hours and no minimum required days on site per month metric
• Comprehensive benefits package and competitive PTO
• Opportunities for career advancement into leadership roles such as Lead CRA or CRA Manager

About the Company

Medpace is a full-service clinical contract research organization (CRO) providing Phase I-IV clinical development services to the biotechnology, pharmaceutical, and medical device industries. Headquartered in Cincinnati, Ohio, Medpace employs over 6,000 people across 40+ countries, leveraging scientific expertise to accelerate the global development of safe and effective medical therapeutics.