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ICON plc
ICON plc
परामर्शलॉजिस्टिक्सस्वास्थ्य सेवा
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।
LinkedIn
कंपनी की नौकरियाँ

Senior Clinical Research Associate – Quebec Remote | ICON plc

Monitor cardiovascular and respiratory clinical trials across Quebec for ICON plc, supporting site compliance, data quality, and adherence to study protocols.

CAकनाडारिमोटपूर्णकालिकजूनियरमध्य स्तरआवश्यक भाषा: अंग्रेज़ीनैदानिक अनुसंधान
Google Cloud Platform

विवरण

  • Manage clinical trial activities in line with study protocols, regulations, and industry standards
  • Lead monitoring work with an emphasis on quality and ongoing process improvement
  • Evaluate site compliance with protocols, regulations, and Good Clinical Practice requirements
  • Perform site visits to review performance, address issues, and support effective study delivery
  • Work with cross-functional teams to coordinate accurate, timely data collection and reporting
  • Train and advise site personnel and fellow Clinical Research Associates
  • Develop and sustain effective working relationships with site teams and study stakeholders
  • Monitor cardiovascular and respiratory studies conducted in Quebec

आवश्यकताएँ

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

लाभ

  • Base salary with performance-based incentives
  • Health and wellness programs, including medical, dental, and vision coverage where applicable
  • Retirement and pension programs
  • Life insurance and disability protection
  • Employee assistance programs and wellbeing support resources
  • Professional development through structured training and career progression pathways

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