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Study Start-Up Coordinator

Canada · Remote · Full-time · Project Management

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About the role

Clinical ResearchCompliance
This position is listed on behalf of a partner company, who manages all applications and next steps. Our partner is looking for a Study Start-Up Coordinator based in Canada. As a Study Start-Up Coordinator, you will play a key role in facilitating the regulatory and administrative processes required to launch clinical research studies successfully. You will oversee regulatory submissions, coordinate with clinical research sites, and ensure that all essential documentation meets Health Canada requirements. Working across diverse clinical trials, therapeutic areas, and study phases, you will collaborate with internal teams and external stakeholders to maintain regulatory compliance and operational efficiency. You will also provide guidance on evolving regulatory requirements and help ensure that study start-up activities are completed accurately and on schedule. This remote opportunity offers exposure to international clinical research projects within a collaborative, quality-driven environment. Your expertise will contribute directly to advancing clinical development and bringing innovative medical treatments closer to patients worldwide.