
5001 - 10000 employees
Founded 1992
🏥 Healthcare
💼 Consulting
📦 Logistics
Healthcare • Consulting • Logistics
Medpace is a full-service contract research organization (CRO) that accelerates the development of safe and effective medical therapeutics. The company offers a comprehensive range of services to biopharmaceutical companies, including clinical trial management, regulatory affairs, and integrated laboratory services. With expertise across various therapeutic areas, Medpace facilitates collaboration among medical professionals to optimize the clinical development process and enhance trial efficiency.
🔥 40 minutes ago
🗣️🇫🇷 French Required
Where this job comes from
Posted on Medpace's careers page, not through a job board
First seen by Remote Rocketship 40 minutes ago

5001 - 10000 employees
Founded 1992
🏥 Healthcare
💼 Consulting
📦 Logistics
Healthcare • Consulting • Logistics
Medpace is a full-service contract research organization (CRO) that accelerates the development of safe and effective medical therapeutics. The company offers a comprehensive range of services to biopharmaceutical companies, including clinical trial management, regulatory affairs, and integrated laboratory services. With expertise across various therapeutic areas, Medpace facilitates collaboration among medical professionals to optimize the clinical development process and enhance trial efficiency.
• 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 interact with clinical research sites • Review patient charts and clinical research data • Participate in customized PACE training and onboarding • Work with international teams of Clinical Research Associates • Support clinical development projects across various therapeutic areas and nationwide site assignments
• Bachelor’s degree in a life science-related field from an accredited university • At least 2 years as a Clinical Research Coordinator • Bilingual in English and French • Thorough knowledge of clinical trial conduct and monitoring methodology under ICH E-6 guidelines and Part C, Division 5 of the Health Canada Food and Drug Regulations • Excellent interpersonal, written, and verbal communication skills in English and French • Strong attention to detail and organizational skills • Highly motivated, independent, and flexible • Ability to travel between 60–70% • Ability to prioritize workload across multiple studies and meet timelines • Proficient in Microsoft Office
• Competitive bonus plans including Resourcing Bonus and Yearly Travel Incentives • Voluntary retirement scheme • Home office furniture allowance • Mobile phone and hotspot for internet access anywhere • In-house travel agents • Reimbursement for airline club and TSA pre-check • Customized PACE training program • Ongoing therapeutic training by in-house physicians • In-house administrative support • No metric for minimum required days on site per month • Flexible work hours across days within a week • Opportunity for CRA leadership positions • Annual team building events and socials • Comprehensive health, wellness, retirement, and PTO benefits • Company-sponsored social events • Office-based culture with occasional work from home that provides flexibility for eligible positions after training • Defined career paths with clear advancement opportunities • Industry-renowned onboarding and training programs • Ongoing training and continuous learning opportunities
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