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medpace
Study Start Up Coordinator
Remote · Canada · Full time · Mid level
About the role
Coordinate study start-up processes remotely, ensuring regulatory compliance and client advisement. Support clinical operations with Health Canada submissions and documentation tracking.
What you’ll do
• Act as contact with sites during study start-up. • Prepare and file clinical trial applications to Health Canada. • Ensure submissions comply with regulations. • Advise study teams on regulatory changes. • Track timely filing of start-up documents.
What you’ll bring
• Proficiency in English required, French preferred. • Ability to work remotely. • Bachelor’s in science or health-related field. • 3-5 years clinical research experience with Health Canada submissions. • Knowledge of ICH guidelines and local regulations. • Work authorization for Canada.
Life at medpace
Offers competitive compensation, comprehensive benefits, continuous learning, and a collaborative culture. Flexible work options after training.
About medpace
Medpace is a global clinical CRO providing phase I-IV development services to biotech, pharmaceutical, and medical device industries.