Associate Business Analyst – Gurugram, India | EXL
EXL
Support business process reviews, requirements documentation, and entry-level data analysis. Work with senior analysts and project teams in a hybrid role based in Gurugram.
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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।
Clinical Site Manager II – Beijing (Hybrid)
Lead site monitoring, compliance, and trial delivery for ICON plc’s sponsor-dedicated clinical research programs in China.
विवरण
- Direct clinical trial operations in line with study protocols, regulations, and industry standards
- Take ownership of technically complex monitoring activities while advancing quality and continuous improvement
- Verify that study sites follow protocols, regulatory obligations, and Good Clinical Practice (GCP) requirements
- Visit sites to evaluate performance, address issues, and help keep trials on track
- Partner with cross-functional teams to support accurate, timely data collection and reporting
- Train and mentor site personnel and fellow Clinical Research Associates
- Develop strong working relationships with investigators, site teams, and other stakeholders
- Coordinate multiple sites and projects concurrently
आवश्यकताएँ
- Bachelor’s degree in a relevant scientific or healthcare-related discipline
- Substantial Clinical Research Associate experience, including a strong command of clinical trial processes and regulatory requirements
- Demonstrated success managing several sites and projects at once, supported by strong organization and problem-solving abilities
- Advanced knowledge of monitoring methods, data integrity, and site management, plus proficiency with applicable clinical trial software and tools
- Strong communication, interpersonal, and stakeholder-management capabilities, with the ability to influence 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 programs, including medical, dental, and vision coverage where applicable
- Retirement and pension benefits
- Life assurance and disability protection
- Employee assistance programs and wellbeing resources
- Professional development through structured training and career progression pathways
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