Local Study Associate Director- FSP

This position is listed on behalf of a partner company, who manages all applications and next steps.

Our partner is looking for a Local Study Associate Director – FSP based in Canada.

This role is a key leadership position within clinical study operations, responsible for driving the successful execution of clinical trials at country level. You will oversee local study teams and ensure that all study activities are delivered on time, within budget, and in compliance with international regulatory standards and Good Clinical Practice (ICH-GCP). Acting as the central point of coordination for site management, you will lead site selection, activation, monitoring, and close-out activities while maintaining strong relationships with investigators, vendors, and global stakeholders. The role requires a high level of operational excellence, strategic oversight, and the ability to manage multiple priorities in a highly regulated environment. You will also contribute to risk management, study planning, and continuous process improvement, playing a direct role in enabling successful clinical development outcomes that ultimately support patient care.

This position is listed on behalf of a partner company, who manages all applications and next steps.

Our partner is looking for a Local Study Associate Director – FSP based in Canada.

This role is a key leadership position within clinical study operations, responsible for driving the successful execution of clinical trials at country level. You will oversee local study teams and ensure that all study activities are delivered on time, within budget, and in compliance with international regulatory standards and Good Clinical Practice (ICH-GCP). Acting as the central point of coordination for site management, you will lead site selection, activation, monitoring, and close-out activities while maintaining strong relationships with investigators, vendors, and global stakeholders. The role requires a high level of operational excellence, strategic oversight, and the ability to manage multiple priorities in a highly regulated environment. You will also contribute to risk management, study planning, and continuous process improvement, playing a direct role in enabling successful clinical development outcomes that ultimately support patient care.

We use an AI-powered matching process to ensure your application is reviewed quickly, objectively, and fairly against the role's core requirements. Our system identifies the top-fitting candidates, and this shortlist is then shared directly with the hiring company. The final decision and next steps (interviews, assessments) are managed by their internal team.

We appreciate your interest and wish you the best!

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