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 Data Manager, Data Standards

Lead clinical data standards, quality, and governance for ICON’s sponsor-dedicated trials. Improve global processes and coordinate delivery across teams.

विवरण

  • Lead the development and implementation of clinical data standards processes and best practices.
  • Drive work on data cleaning, data quality, edit checks, data listings, and standards library management.
  • Work closely with Clinical Trial Reporting (CTR), Clinical Trial Configuration (CTC), and Cross-Functional Data Review (CFDR) teams.
  • Set governance, workflows, and quality standards that support clinical trial delivery.
  • Lead and mentor Associate Manager-level colleagues and encourage continuous improvement.
  • Work with cross-functional stakeholders to turn strategic objectives into operational plans.
  • Identify risks, improve processes, and advance data quality throughout the clinical data lifecycle.

आवश्यकताएँ

  • Hold a bachelor’s degree in life sciences, health sciences, or a related field.
  • Bring extensive clinical data management experience from a CRO, biotechnology, or pharmaceutical setting.
  • Have strong experience in process development, project management, stakeholder engagement, and cross-functional collaboration.
  • Show a proven ability to build and implement new processes and ways of working.
  • Have experience with data quality, standards development, data review, edit checks, data listings, or standards library management.
  • Understand clinical trial processes, regulatory requirements, and ICH-GCP.
  • Demonstrate strong communication, problem-solving, and leadership skills.
  • Bring an entrepreneurial outlook and the ability to thrive in a developing, evolving function.
  • Have legal authorization to work in the country where the role is based.

लाभ

  • Competitive base pay with performance-related incentives.
  • Health and wellbeing programmes, including medical, dental, and vision coverage where applicable.
  • Retirement and pension plans.
  • Life assurance and disability coverage.
  • Employee assistance programmes and wellbeing resources.
  • Learning and development through structured training and career pathways.

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