Clinical Study Administrator

This position is listed on behalf of a partner company, who manages all applications and next steps. Our partner is looking for a Clinical Study Administrator based in Canada.

This role plays a key part in the smooth coordination and execution of clinical research activities that contribute directly to the development of new therapies and improved patient outcomes. You will support clinical trial operations from start-up through to close-out, ensuring documentation, compliance, and communication processes are managed with accuracy and efficiency. Working within a collaborative Local Study Team, you will interact with investigators, clinical research associates, and external partners in a fast-paced, regulated environment. The position requires strong organizational skills, attention to detail, and the ability to manage multiple priorities while maintaining compliance with international clinical standards. It is an opportunity to contribute to meaningful healthcare innovation while supporting high-quality study delivery. The role is based in Ontario with a hybrid arrangement requiring on-site presence three days per week.

This position is listed on behalf of a partner company, who manages all applications and next steps. Our partner is looking for a Clinical Study Administrator based in Canada.

This role plays a key part in the smooth coordination and execution of clinical research activities that contribute directly to the development of new therapies and improved patient outcomes. You will support clinical trial operations from start-up through to close-out, ensuring documentation, compliance, and communication processes are managed with accuracy and efficiency. Working within a collaborative Local Study Team, you will interact with investigators, clinical research associates, and external partners in a fast-paced, regulated environment. The position requires strong organizational skills, attention to detail, and the ability to manage multiple priorities while maintaining compliance with international clinical standards. It is an opportunity to contribute to meaningful healthcare innovation while supporting high-quality study delivery. The role is based in Ontario with a hybrid arrangement requiring on-site presence three days per week.

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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