Senior Study Start-Up Specialist

This position is listed on behalf of a partner company, who manages all applications and next steps. Our partner is looking for a Senior Study Start-Up Specialist based in Canada.

• This role is responsible for driving high-quality study start-up activities across clinical research programs.
• You will coordinate site activation from selection through initiation, helping keep studies on track and within established timelines.
• The position combines regulatory submissions, document management, site engagement, and clinical systems expertise.
• You will work closely with cross-functional teams and site partners to streamline processes and reduce start-up cycle times.
• The role also contributes to improving study start-up infrastructure, workflows, and operational efficiency across North America.
• Success requires strong attention to detail, sound knowledge of clinical research regulations, and effective stakeholder communication.
• This is an opportunity to contribute to clinical development in a collaborative, fast-moving, and purpose-driven environment.