Study Startup Coordinator
3 weeks ago
Our clinical operations activities are growing rapidly, and we are currently seeking a full-time, remote-based Regulatory Submissions Coordinator to join our Clinical Operations team. As a Regulatory Submissions Coordinator with Medpace Canada, you will have the opportunity to work with innovative therapeutic fields with exposure to diverse, challenging studies ranging from Phases I – III. With our continued growth in Canada, we are looking for proactive, positive, and self-motivated individuals with a shared commitment to quality to join our supportive and dynamic team.
Act as the point of contact with sites during the study start up process;
Proficiency in English and French;
Ability to work in a remote setting;
Bachelor’s degree in a science or health-related field;
Knowledge of ICH guidelines and applicable local regulations; 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. Hybrid work-from-home options (dependent upon position and level)
Flexible work schedule
Continually recognized with CRO Leadership Awards from Life Science Leader magazine based on expertise, quality, capabilities, reliability, and compatibility
EO/AA Employer M/F/Disability/Vets
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