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 Trial Manager - Mexico Remote

Lead end-to-end clinical trial delivery for ICON plc, including study oversight, enrollment, budgets, start-up, and regulatory compliance. Guide cross-functional teams and support successful outcomes across complex clinical research programs.

विवरण

  • Lead the planning, execution, and completion of clinical trials
  • Maintain compliance with study timelines, budgets, and regulatory requirements
  • Coordinate clinical trial delivery, resolve operational issues, and strengthen team capabilities
  • Manage the clinical budget and allocate resources efficiently
  • Create monitoring plans and tools to support effective study oversight
  • Train and mentor Clinical Research Associates (CRAs)
  • Drive participant enrollment and lead study start-up activities
  • Review trip reports and introduce corrective and preventive action plans when needed
  • Build effective working relationships with sponsors, vendors, and cross-functional teams
  • Provide strategic direction to support successful clinical trial outcomes

आवश्यकताएँ

  • At least 4 years of Clinical Trial Management experience within a CRO or pharmaceutical organization
  • A bachelor's degree in health sciences, life sciences, or a related field
  • At least 10 years of relevant clinical trial management experience
  • Monitoring experience of 2 or more years is preferred
  • Experience supporting complex protocols, such as MASH/NASH, radiopharmaceutical, or other specialized therapeutic programs, is highly valued
  • Experience managing complex or global clinical trials is advantageous
  • Experience overseeing all trial components from start-up through database lock is preferred
  • This position is for experienced CTM professionals; entry-level CTM experience alone is insufficient
  • Willingness to travel approximately 25% as required
  • Legal authorization to work in the country where the role is based

लाभ

  • Competitive 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 pathways supporting learning and development

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