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।

Clinical Research Associate – Canada Remote | ICON plc

Monitor respiratory and cardiovascular clinical trials for ICON Strategic Solutions across Canada's Greater Toronto Area. Coordinate site visits, compliance, data quality, and guidance for clinical research teams.

विवरण

  • Manage clinical trial activities in line with study protocols, regulations, and industry standards
  • Drive monitoring activities focused on quality and ongoing process improvement
  • Evaluate site compliance with protocols, regulations, and Good Clinical Practice requirements
  • Complete site visits to review performance, address issues, and support effective study delivery
  • Partner with cross-functional teams to ensure accurate, timely data collection and reporting
  • Train and advise site staff and fellow Clinical Research Associates
  • Develop and sustain productive relationships with site teams and other stakeholders
  • Monitor respiratory and cardiovascular studies throughout the Greater Toronto Area

आवश्यकताएँ

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

लाभ

  • Competitive base pay with performance-based incentives
  • Health and wellness programs, including medical, dental, and vision coverage where available
  • Retirement and pension provisions
  • Life insurance and disability protection
  • Employee assistance programs and wellbeing resources
  • Structured training, professional development, and career progression opportunities

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