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Clinical Research Associate - Vancouver Onsite

Manage compliant clinical trial execution for Novo Nordisk in Vancouver, with responsibility for site monitoring, risk management, patient safety, and data integrity.

CAKanada
85 500 $ – 135 500 $ / yil
OfisdaTo‘liq stavkaJuniorO‘rta darajaTalab Qilinadigan Til: inglizchaKlinik tadqiqot
Google Cloud Platform

Tavsif

  • Manage assigned clinical trial sites through on-site and remote monitoring visits.
  • Maintain compliance with study protocols, ICH-GCP, and applicable regulatory requirements.
  • Use Risk-Based Quality Management (RBQM) to identify, evaluate, and proactively mitigate study risks.
  • Monitor site performance, recruitment, retention, and data collection.
  • Investigate discrepancies and manage adverse events to safeguard patient safety and data integrity.
  • Maintain site readiness for inspections.
  • Train and support site personnel on protocols, procedures, systems, and compliance obligations.
  • Represent Novo Nordisk at the site level while developing effective relationships with investigators and site teams.
  • Work with cross-functional colleagues to support clinical trial delivery.
  • Advance study operations through continuous improvement, new technologies, and digital tools.

Talablar

  • Bachelor’s degree in Life Sciences or a related discipline.
  • At least one year of experience in clinical trial monitoring or a relevant pharmaceutical or CRO position.
  • Knowledge of ICH-GCP, regulatory requirements, and clinical trial methodology.
  • Demonstrated delivery of high-quality trial activities in accordance with ICH-GCP, regulations, and internal SOPs.
  • Practical experience with clinical trial platforms including EDC, CTMS, and eTMF.
  • Strong organisational, time management, and project management capabilities.
  • Ability to oversee multiple sites and competing priorities with close attention to detail.
  • Sound problem-solving and decision-making skills, including the ability to identify and mitigate risks.
  • Excellent written and verbal communication skills.
  • Ability to establish effective relationships with internal and external stakeholders.
  • Capacity to work independently and collaboratively in a dynamic environment.
  • High integrity and a consistent commitment to quality and patient safety.
  • Willingness to adopt new technologies and digital tools.
  • Availability to travel up to 70% of the time.
  • Practical experience applying Risk-Based Quality Management (RBQM) in study conduct.

Imtiyozlar

  • Ongoing learning opportunities
  • Support for career progression
  • Benefits aligned with your life and career stage
  • Short-term incentive (STI) opportunities may apply
  • Long-term incentive (LTI) opportunities may apply

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