Clinical Trials Site Monitor & Quality Guardian

Novo Nordisk A/S; Vancouver; Vor Ort; CAD 86.000 - 136.000; Vollzeit

Zusammenfassung

Novo Nordisk A/S in Canada is seeking a Clinical Research Associate to ensure clinical trials at assigned sites run to high standards of quality, compliance and patient safety. You will monitor progress, spot risks early and help sites deliver reliable data on time.

You will own day-to-day site oversight, conduct on-site and remote monitoring visits, apply risk-based quality management principles, track performance and train site staff while building strong investigator relationships.

Qualifikationen

• Bachelor’s degree in Life Sciences or related field.
• 1+ years in clinical trial monitoring or related pharma/CRO role.
• Strong knowledge of ICH-GCP, regulatory requirements.
• Experience with EDC, CTMS, and eTMF systems.
• Ability to travel up to 70%.

Aufgaben

• Oversee day-to-day site monitoring and data quality.
• Apply RBQM principles to identify and mitigate risks.
• Track site performance, recruitment and data collection.
• Ensure patient safety and data integrity; manage adverse events.
• Train site staff on protocols and systems.
• Represent Novo at site level and build relationships.

Kenntnisse

Organization

Project management

Time management

Communication

Problem-solving

Ausbildung

Bachelor’s degree in Life Sciences or related field

Tools

EDC

CTMS

eTMF

Jobbeschreibung

Novo Nordisk A/S in Canada is seeking a Clinical Research Associate to ensure clinical trials at assigned sites run to high standards of quality, compliance and patient safety. You will monitor progress, spot risks early and help sites deliver reliable data on time.

You will own day-to-day site oversight, conduct on-site and remote monitoring visits, apply risk-based quality management principles, track performance and train site staff while building strong investigator relationships.