Job opportunity
Study Start-Up Coordinator Canada
Jobgether
Support clinical trial launches remotely from Canada through Health Canada submissions and precise regulatory documentation coordination. Help activate studies across international research projects.
As a Study Start-Up Coordinator, you will facilitate regulatory and administrative activities across clinical trials, therapeutic areas, and study phases. You will coordinate with clinical research sites, internal teams, and external stakeholders while maintaining compliance with Canadian regulations, ICH-GCP guidelines, and study timelines. This position contributes to accurate, efficient study activation.
Key Responsibilities:
Serve as primary contact for clinical research sites
Prepare and submit clinical trial applications to Health Canada
Review regulatory documents for compliance with Canadian requirements
Track essential documentation and monitor submission progress
Advise study teams on evolving regulatory obligations
Requirements:
Bachelor's degree in scientific, life sciences, or health discipline
Three to five years of clinical research experience
Hands-on Health Canada and Research Ethics Board submission experience
Knowledge of ICH-GCP and local clinical research regulations
Strong organization, communication, and remote collaboration skills
Apply your Health Canada submissions, site coordination, and regulatory expertise to support accurate clinical study activation across Canada.
#J-18808-Ljbffr
Apply on source site As a Study Start-Up Coordinator, you will facilitate regulatory and administrative activities across clinical trials, therapeutic areas, and study phases. You will coordinate with clinical research sites, internal teams, and external stakeholders while maintaining compliance with Canadian regulations, ICH-GCP guidelines, and study timelines. This position contributes to accurate, efficient study activation.
Key Responsibilities:
Serve as primary contact for clinical research sites
Prepare and submit clinical trial applications to Health Canada
Review regulatory documents for compliance with Canadian requirements
Track essential documentation and monitor submission progress
Advise study teams on evolving regulatory obligations
Requirements:
Bachelor's degree in scientific, life sciences, or health discipline
Three to five years of clinical research experience
Hands-on Health Canada and Research Ethics Board submission experience
Knowledge of ICH-GCP and local clinical research regulations
Strong organization, communication, and remote collaboration skills
Apply your Health Canada submissions, site coordination, and regulatory expertise to support accurate clinical study activation across Canada.
#J-18808-Ljbffr