Job Description
This position is listed on behalf of a partner company, who manages all applications and next steps. Our partner is looking for a Senior Clinical Research Associate based in Canada.
This role offers the opportunity to play a key part in advancing clinical development programs that directly contribute to improving patient outcomes worldwide.
You will act as a critical link between clinical trial sites and study operations, ensuring that studies are conducted in compliance with protocol requirements, ICH-GCP standards, and applicable regulatory guidelines.
The position involves extensive collaboration with investigators and site teams to support study execution, resolve operational challenges, and maintain high-quality data integrity.
You will take ownership of site performance across all study phases, from initiation through close-out, while ensuring timely delivery of milestones and study objectives.
Working in a dynamic, matrixed environment, you will contribute to both onsite and remote monitoring activities, supporting global clinical trials with precision and accountability.
This role is well-suited for a proactive clinical research professional who thrives in a fast-paced, quality-driven environment and is passionate about advancing healthcare innovation.
This position is listed on behalf of a partner company, who manages all applications and next steps. Our partner is looking for a Senior Clinical Research Associate based in Canada.
This role offers the opportunity to play a key part in advancing clinical development programs that directly contribute to improving patient outcomes worldwide.
You will act as a critical link between clinical trial sites and study operations, ensuring that studies are conducted in compliance with protocol requirements, ICH-GCP standards, and applicable regulatory guidelines.
The position involves extensive collaboration with investigators and site teams to support study execution, resolve operational challenges, and maintain high-quality data integrity.
You will take ownership of site performance across all study phases, from initiation through close-out, while ensuring timely delivery of milestones and study objectives.
Working in a dynamic, matrixed environment, you will contribute to both onsite and remote monitoring activities, supporting global clinical trials with precision and accountability.
This role is well-suited for a proactive clinical research professional who thrives in a fast-paced, quality-driven environment and is passionate about advancing healthcare innovation.