ICON plc sog‘liqni saqlash va farmatsevtika sohalariga xizmat ko‘rsatuvchi global shartnoma asosidagi tadqiqot tashkilotidir. Kompaniya faoliyati dastlabki tadqiqotlardan tortib, marketingdan keyingi jarayonlargacha dori vositalarini ishlab chiqishni qo‘llab-quvvatlovchi klinik, konsalting va tijoriy xizmatlarni qamrab oladi. ICON plc markazlashtirilmagan klinik sinovlar, yurak xavfsizligi, dastlabki klinik laboratoriyalar, tibbiy tasvirlash, tartibga solish bo‘yicha ma’lumotlar va real hayot ma’lumotlari kabi yechimlarni taqdim etadi. Shuningdek, kompaniya yurak-qon tomir kasalliklari, onkologiya, ichki kasalliklar, hujayra va gen terapiyalari hamda biosimilyarlar kabi yo‘nalishlarda terapevtik tajribaga ega bo‘lib, klinik dasturlarni rivojlantirishga yordam berish uchun ma’lumotlar tahlilini bemorga yo‘naltirilgan yondashuvlar bilan birlashtiradi.
Senior Clinical Research Associate – Phase I Oncology (Remote, United States)
ICON plc is hiring a Senior Clinical Research Associate to monitor sponsor-dedicated Phase I oncology trials remotely from the United States. The role oversees sites, maintains GCP compliance, and supports clinical trial teams.
Tavsif
- Manage clinical trial activities in line with study protocols, regulations, and industry standards
- Lead monitoring activities with an emphasis on quality and ongoing process improvement
- Evaluate site compliance with protocols, regulatory obligations, and GCP requirements
- Conduct site visits to review performance, address issues, and support effective study delivery
- Partner with cross-functional teams to ensure accurate, timely data collection and reporting
- Train and mentor site personnel and fellow Clinical Research Associates
- Develop and maintain effective working relationships with site teams and key stakeholders
- Support sponsor-dedicated Phase I oncology studies
Talablar
- Bachelor’s degree in a relevant scientific or healthcare discipline
- Substantial experience working as a Clinical Research Associate
- Thorough knowledge of clinical trial procedures and regulatory requirements
- Demonstrated ability to manage multiple sites and projects concurrently
- Strong organizational, analytical, and problem-solving capabilities
- Advanced knowledge of monitoring procedures, data integrity, and site management
- Proficiency with relevant clinical trial software and tools
- Excellent communication, interpersonal, and stakeholder management abilities
- Availability to travel as needed, approximately 60%
- Current experience monitoring oncology studies
- Legal authorization to work in the country where the role is based
Imtiyozlar
- Competitive base pay with performance-linked incentives
- Health and wellbeing programs, including medical, dental, and vision coverage where applicable
- Retirement and pension plans
- Life insurance and disability coverage
- Employee assistance programs and wellbeing resources
- Structured training, learning, and career development opportunities