ICON plc
ICON plc
ICON plc स्वास्थ्य सेवा और फार्मास्युटिकल उद्योगों को सेवाएँ प्रदान करने वाला एक वैश्विक कॉन्ट्रैक्ट रिसर्च संगठन है। इसका कार्य क्लिनिकल, परामर्श और वाणिज्यिक सेवाओं तक फैला है, जो शुरुआती अनुसंधान से लेकर विपणन-पश्चात गतिविधियों तक दवा विकास में सहायता करती हैं। कंपनी विकेंद्रीकृत क्लिनिकल परीक्षण, हृदय सुरक्षा, प्रारंभिक क्लिनिकल प्रयोगशालाएँ, मेडिकल इमेजिंग, नियामक इंटेलिजेंस और वास्तविक-विश्व साक्ष्य जैसी सेवाएँ प्रदान करती है। ICON plc हृदय रोग, ऑन्कोलॉजी, आंतरिक चिकित्सा, सेल और जीन थेरेपी तथा बायोसिमिलर जैसे क्षेत्रों में चिकित्सीय विशेषज्ञता भी उपलब्ध कराती है। डेटा विश्लेषण और रोगी-केंद्रित दृष्टिकोणों को मिलाकर कंपनी क्लिनिकल कार्यक्रमों को आगे बढ़ाने में मदद करती है।

Senior Clinical Research Associate - Canada Remote

ICON plc is seeking a Senior Clinical Research Associate to monitor respiratory and cardiovascular trials across the Greater Toronto Area. The role oversees site performance, regulatory compliance, data quality, and trial delivery.

विवरण

  • Manage clinical trial activities in line with study protocols, regulations, and industry standards
  • Direct technically complex monitoring activities while advancing quality and continuous improvement
  • Evaluate site compliance with protocols, regulations, and Good Clinical Practice (GCP) requirements
  • Conduct site visits to review performance, address issues, and support effective trial delivery
  • Partner with cross-functional teams to maintain accurate, timely data collection and reporting
  • Train and support site personnel and fellow Clinical Research Associates
  • Develop productive relationships with site teams and stakeholders to support efficient trial operations
  • Monitor respiratory and cardiovascular studies throughout the Greater Toronto Area

आवश्यकताएँ

  • Bachelor’s degree in a relevant scientific or healthcare-related discipline
  • Extensive Clinical Research Associate experience with a strong grasp of clinical trial processes and regulatory obligations
  • Demonstrated ability to oversee multiple sites and projects while applying strong organization and problem-solving skills
  • Advanced knowledge of monitoring methods, data integrity, and site management
  • Proficiency with relevant clinical trial software and tools
  • Strong communication, interpersonal, and stakeholder management capabilities, including the ability to influence compliance in complex settings
  • Availability to travel as needed, approximately 60%
  • Legal authorization to work in the country where the position is based

लाभ

  • Base salary with performance-based incentives
  • Health and wellbeing programmes, including medical, dental, and vision coverage where applicable
  • Retirement and pension programmes
  • Life assurance and disability coverage
  • Employee assistance programmes and wellbeing resources
  • Structured training and career development opportunities

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