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 - France Remote | ICON plc
Senior Clinical Research Associate overseeing clinical trial monitoring for ICON plc’s sponsor-dedicated research programs in France. The role focuses on protocol compliance, site performance, data quality, and regulatory standards.
विवरण
- Manage clinical trial activities in line with study protocols, regulations, and industry standards
- Lead technically complex monitoring work while advancing quality and process improvement
- Evaluate clinical trial sites against protocols, regulations, and Good Clinical Practice requirements
- Conduct site visits, address operational issues, and support effective study delivery
- Partner with cross-functional teams to ensure accurate, timely data collection and reporting
- Train and mentor site staff and fellow Clinical Research Associates
- Develop strong working relationships with site teams and stakeholders to support efficient trial operations
आवश्यकताएँ
- Bachelor’s degree in a relevant scientific or healthcare discipline
- Substantial Clinical Research Associate experience with strong knowledge of trial operations and regulatory requirements
- Demonstrated ability to coordinate multiple sites and projects, supported by strong organization and problem-solving skills
- Advanced knowledge of monitoring methods, data integrity, and site management, including relevant clinical trial systems and tools
- Strong communication, interpersonal, and stakeholder-management abilities, with the influence needed 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
- Competitive base pay with performance-based incentives
- Health and wellbeing programmes, including medical, dental, and vision coverage where applicable
- Retirement and pension arrangements
- Life assurance and disability protection
- Employee assistance programmes and wellbeing support
- Professional development through structured training and career progression pathways