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, 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.
Tavsif
- 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
Talablar
- 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
Imtiyozlar
- 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