Jobgether

Associate Site Manager

Canada

Sponsorship not specified$72k-$116kDetected 1 day ago

GCPComplianceClinical TrialsClinical ResearchResearchCommunicationCollaborationProblem SolvingTime ManagementGxP

About the role

You will serve as a key connection between investigators, study teams, and healthcare professionals throughout the clinical trial lifecycle.
The role is ideal for a detail-oriented clinical research professional who enjoys working independently while contributing to meaningful medical advancements.
Our system identifies the top-fitting candidates, and this shortlist is then shared directly with the hiring company.

This position is listed on behalf of a partner company, who manages all applications and next steps.
Our partner is looking for an Associate Site Manager based in Canada.
You will manage relationships with clinical trial sites, ensuring studies are conducted safely, efficiently, and in compliance with regulatory standards.
The position combines site management, patient recruitment support, monitoring activities, and collaboration with global clinical operations teams.
You will gain exposure to diverse therapeutic areas while developing expertise in clinical trial operations within a field-based environment.
Act as the primary point of contact for assigned clinical trial sites and maintain strong relationships with investigators, coordinators, and study teams.
Support site selection, initiation, maintenance, and close-out activities across Phase 1-4 clinical trials.
Perform source document verification, Investigator Site File reviews, drug accountability checks, and other monitoring activities to ensure data integrity and compliance.
Support patient recruitment strategies and collaborate with sites to help achieve enrollment goals and study timelines.
Identify, manage, and escalate site-specific issues while partnering with investigators and internal teams to drive timely resolutions.

Bachelor's degree in Biological Sciences or a related scientific field, or equivalent qualification.
Strong understanding of Good Clinical Practice (GCP), ICH guidelines, and local regulatory requirements.
Experience with clinical trial systems and databases such as CTMS, EDC, TMF, IWRS, safety reporting platforms, and study dashboards.

Previous experience in pharmaceutical, biotechnology, or clinical research environments is preferred.
Knowledge of risk-based monitoring approaches and clinical trial quality practices is highly preferred.

Competitive annual base salary range of approximately $72,000-$116,150 CAD, depending on skills, experience, and qualifications.

Eligibility for a discretionary performance bonus.
Opportunity to contribute to impactful clinical research programs and healthcare innovation.
Professional growth opportunities within a leading healthcare research environment.
This role offers the opportunity to support the delivery of innovative clinical research programs that help advance new healthcare solutions.
Field-based and remote work flexibility with home office support.

We use an AI-powered matching process to ensure your application is reviewed quickly, objectively, and fairly against the role's core requirements.
The final decision and next steps (interviews, assessments) are managed by their internal team.
We appreciate your interest and wish you the best!
Why Apply Through Jobgether?

This listing is sourced directly from Jobgether's careers page and normalized into a canonical job model.