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 – South Africa (Remote)

Senior Clinical Research Associate overseeing site monitoring and trial execution for ICON’s sponsor-dedicated research programs. The role focuses on protocol compliance, site performance, data quality, and regulatory standards.

विवरण

  • Support sponsor-dedicated research programs using ICON’s global clinical expertise
  • Manage clinical trial activities in line with protocols, regulations, and industry standards
  • Lead technically complex monitoring work with a focus on quality and ongoing improvement
  • Evaluate site adherence to study protocols, regulatory requirements, and Good Clinical Practice standards
  • Conduct site visits to review performance, address issues, and help deliver trials successfully
  • Partner with cross-functional teams to support timely, accurate data collection and reporting
  • Train and advise site staff and fellow Clinical Research Associates
  • Develop relationships with site personnel and stakeholders to support efficient trial operations

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 requirements
  • Demonstrated ability to coordinate multiple sites and projects while applying strong organization and problem-solving skills
  • Advanced knowledge of monitoring methods, data integrity, and site management, including relevant clinical trial software and tools
  • Strong communication, interpersonal, and stakeholder management abilities, with the capacity to influence compliance in a complex environment
  • Availability to travel as needed, approximately 60% of the time
  • Legal authorization to work in the country where the role is located

लाभ

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

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