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 – California Remote
Lead Phase I oncology trial monitoring for ICON’s sponsor-dedicated research programs. Oversee sites, compliance, data integrity, and clinical research associate guidance.
संयुक्त राज्य
कैलिफ़ोर्निया$1,10,520 – $1,38,150 / वर्ष
रिमोटपूर्णकालिकवरिष्ठआवश्यक भाषा: अंग्रेज़ीनैदानिक अनुसंधानविवरण
- Manage clinical trial activities in line with protocols, regulations, and industry standards
- Lead technically complex monitoring work focused on quality and continuous improvement
- Assess site compliance with study protocols, regulations, and Good Clinical Practice standards
- Conduct site visits to evaluate performance, resolve issues, and support trial delivery
- Partner with cross-functional teams to ensure accurate, timely data collection and reporting
- Train and support site staff and other clinical research associates
- Maintain effective working relationships with site personnel and study stakeholders
आवश्यकताएँ
- Bachelor’s degree in a relevant scientific or healthcare-related discipline
- Extensive Clinical Research Associate experience with strong knowledge of clinical trial processes and regulatory requirements
- Demonstrated ability to manage multiple sites and projects while applying strong organizational and problem-solving skills
- Advanced knowledge of monitoring practices, data integrity, and site management, including relevant clinical trial software and tools
- Excellent communication, interpersonal, and stakeholder management abilities, with the capacity to influence compliance in complex environments
- Willingness to travel approximately 60% as required
- Current oncology monitoring experience
- 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 development opportunities