Accelerating Drug, Biologic and Medical Device Clinical Development
Cincinnati, OH
Medpace is a scientifically-driven, global, full-service clinical contract research organization (CRO) providing Phase I-IV clinical development services to the biotechnology, pharmaceutical and medical device industries. Medpace’s mission is to accelerate the global development of safe and effective medical therapeutics through its high-science and disciplined operating approach that leverages local regulatory and deep therapeutic expertise across all major areas including oncology, cardiology, metabolic disease, endocrinology, central nervous system and anti-viral and anti-infective. Headquartered in Cincinnati, Ohio, Medpace employs approximately 6,500 people across 46 countries.
Remote · Alberta, Canada, British Columbia, Canada
Conduct pre-study, initiation, monitoring, and closeout visits for research sites in accordance with SOPs and GCP guidelines. Maintain site correspondence, manage study-related databases, and perform oversight of clinical research data and patient charts.
Remote · Montreal, Quebec, Canada
The Clinical Research Associate conducts pre-study, initiation, monitoring, and closeout visits for research sites while maintaining site correspondence and study-related databases. They are responsible for overseeing clinical research sites and reviewing patient charts and clinical research data to ensure compliance with SOPs and GCP.
Remote · Canada
The Associate Director manages day-to-day clinical trial operations, ensuring compliance with ICH/GCP regulations and study protocols. They serve as the primary sponsor contact, oversee cross-functional project teams, and manage study deliverables, risk assessments, and vendor relationships.
