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Novo Nordisk
Novo Nordisk
H1B वीज़ा प्रायोजकखाद्य और पेयपरामर्शस्वास्थ्य सेवा
Novo Nordisk एक वैश्विक स्वास्थ्य सेवा कंपनी है, जो मोटापे और मधुमेह के उपचार विकसित करने पर केंद्रित है और इन क्षेत्रों में 25 से अधिक वर्षों से अनुसंधान कर रही है। 1923 में स्थापित यह कंपनी जीवन के विभिन्न चरणों में रोगियों की सहायता के लिए बनाई गई दवाओं का उत्पादन करती है और नकली दवाओं से निपटने के प्रयासों सहित अपने उत्पादों की सुरक्षा और विश्वसनीयता को मजबूत करने के लिए काम करती है। इसका कार्य औषधीय अनुसंधान, रोगी देखभाल और आवश्यक उपचार तक पहुंच में सुधार के व्यापक प्रयासों तक फैला हुआ है।
LinkedIn
कंपनी की नौकरियाँ

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.

CAकनाडा
$85,500 – $1,35,500 / वर्ष
ऑन-साइटपूर्णकालिकजूनियरमध्य स्तरआवश्यक भाषा: अंग्रेज़ीनैदानिक अनुसंधान
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विवरण

  • 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.

आवश्यकताएँ

  • 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.

लाभ

  • 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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