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IQVIA
IQVIA
H1B vizasi homiysiIshlab chiqarishKonsaltingMarketing
IQVIA hayot fanlari va sog‘liqni saqlash sohalaridagi tashkilotlarga murakkab muammolarni hal qilishda yordam berish uchun sog‘liqni saqlash ma’lumotlari tahlili, ilg‘or texnologiyalar va konsaltingni birlashtiradi. Uning Connected Intelligence platformasi klinik tadqiqotlar, texnologiyalarni ishlab chiqish va yangi davolash usullarini rivojlantirishni qo‘llab-quvvatlash uchun ma’lumotlar hamda sun’iy intellektni birlashtiradi. Kompaniya jamoalari tahlil, konsalting va sog‘liqni saqlash texnologiyalari yo‘nalishlarida faoliyat yuritib, tadqiqotlar, raqamli innovatsiyalar va bemorlar natijalarini yaxshilashga qaratilgan sa’y-harakatlar bilan bog‘liq imkoniyatlarni taqdim etadi.
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Kompaniyadagi ish o‘rinlari

Clinical Research Associate - Hybrid in Melbourne

Support clinical trial sites and study data for IQVIA in Australia. The role covers recruitment, compliance, documentation, monitoring, and trial delivery.

AUAvstraliyaGibridTo‘liq stavkaJuniorO‘rta darajaTalab Qilinadigan Til: inglizchaKlinik tadqiqot
Google Cloud Platform

Tavsif

  • Oversee site monitoring and management to ensure study conduct and data reporting meet protocols, regulations, guidelines, and sponsor requirements.
  • Conduct site visits across selection, initiation, monitoring, and close-out stages.
  • Implement, advance, and monitor subject recruitment plans.
  • Deliver protocol and study training to assigned sites while maintaining regular site communication.
  • Assess site practices for protocol and regulatory compliance, escalating quality concerns as needed.
  • Monitor regulatory submissions, approvals, recruitment, enrollment, CRF completion, and the creation and resolution of data queries.
  • Assist with study start-up activities when required.
  • Maintain Trial Master File documentation and confirm that Investigator Site Files are properly maintained.
  • Record site-management activities, monitoring findings, and action plans in visit reports and follow-up correspondence.
  • Work with study team members to support project delivery.
  • Help create site-specific subject recruitment plans when required.
  • Oversee site finances and collect invoices in line with local requirements when required.

Talablar

  • Bachelor’s degree in a scientific or healthcare discipline, or an equivalent combination of education, training, and experience.
  • At least nine months of independent on-site monitoring experience.
  • Working knowledge of clinical research regulations, including GCP and ICH guidelines.
  • Working therapeutic-area and protocol knowledge gained through company training.
  • Proficiency with Microsoft Word, Excel, and PowerPoint.
  • Ability to use a laptop, iPhone, and iPad when required.
  • Strong organizational and problem-solving abilities.
  • Effective time and financial management skills.
  • Ability to build and maintain productive relationships with colleagues, managers, and clients.

Imtiyozlar

  • Competitive salary plus car and health allowances.
  • Flexible hybrid working arrangement.
  • Career development opportunities across FSO and FSP models.
  • Opportunity to work with experienced managers across clinical trials in multiple phases.

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