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, Medical Device — Remote, United States
Senior Clinical Research Associate overseeing orthopedic medical-device trials for ICON Strategic Solutions. The role covers site monitoring, compliance, data integrity, and trial execution across Midwest and Western regions.
संयुक्त राज्य
इलिनॉय
मिसौरी
नेब्रास्का
ओक्लाहोमा
टेक्सास$1,10,520 – $1,38,150 / वर्ष
रिमोटपूर्णकालिकवरिष्ठआवश्यक भाषा: अंग्रेज़ीनैदानिक अनुसंधानविवरण
- Manage clinical trial activities in line with study protocols, regulations, and industry standards
- Lead technically complex monitoring work with an emphasis on quality and ongoing improvement
- Evaluate clinical sites for compliance with protocols, regulations, and Good Clinical Practice standards
- Conduct site visits to review performance, address issues, and support effective study delivery
- Partner with cross-functional teams to ensure clinical data and reports are collected accurately and on schedule
- Train and advise site personnel and fellow Clinical Research Associates
- Develop and sustain effective working relationships with site teams and other stakeholders
- Coordinate multiple clinical sites and projects at the same time
आवश्यकताएँ
- Bachelor’s degree in a relevant scientific or healthcare discipline
- Three to five years of Clinical Research Associate monitoring experience in CRO or pharmaceutical settings
- Demonstrated experience managing complex clinical protocols
- Substantial Clinical Research Associate experience and a strong command of clinical trial processes and regulatory obligations
- Track record of managing several sites and projects concurrently
- Advanced knowledge of monitoring methods, data integrity, and site management
- Working knowledge of applicable clinical trial software and tools
- Strong communication, relationship-building, and stakeholder management abilities
- Availability for approximately 60% travel as required
- Some travel to Canada may be required
- Legal authorization to work in the country where the position is based
लाभ
- Base salary with performance-based incentive opportunities
- Medical, dental, and vision coverage through health and wellbeing programs where applicable
- Retirement and pension arrangements
- Life insurance and disability protection
- Employee assistance programs and wellbeing support resources
- Structured training and career development opportunities