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Linical
Linical
501 – 1 000 Xodimlar
KonsaltingLogistikaSog‘liqni saqlash
Linical dori vositalarini ishlab chiqish jarayonining barcha bosqichlarida biofarmatsevtika kompaniyalariga xizmat ko‘rsatuvchi global klinik tadqiqot tashkilotidir. Uning faoliyati onkologiya, nevrologiya, psixiatriya, immunologiya va endokrinologiya kabi terapevtik yo‘nalishlarda klinik ishlab chiqish strategiyasi, protokol tuzish, tartibga solish masalalari bo‘yicha maslahat, bemorlarni jalb qilish va tadqiqotlarni boshqarishni qamrab oladi. Linical xalqaro qamrovini moslashtirilgan ko‘mak va ma’lumotlarni ishonchli yig‘ishga qaratilgan yondashuv bilan birlashtirib, mijozlarga operatsion muammolarni hal qilish hamda butun dunyo bo‘ylab bemorlar uchun yangi davolash usullariga qaratilgan murakkab klinik tadqiqotlarni ilgari surishda yordam beradi.
LinkedIn
Kompaniyadagi ish o‘rinlari

Clinical Trial Associate — United States (Remote)

Support Linical’s clinical research programs through trial documentation, TMF administration, regulatory submissions, site support, and coordination with study teams.

USAmerika Qo‘shma Shtatlari
50 000 $ – 70 000 $ / yil
MasofaviyTo‘liq stavkaJuniorO‘rta darajaTalab Qilinadigan Til: inglizchaKlinik sinovlar bo'yicha yordamchiUmumiy
Google Cloud PlatformVault

Tavsif

  • Provide administrative support across the clinical project team
  • Support the Project Manager with communications involving study teams and sites
  • Assist with site identification and feasibility assessments
  • Gather initial essential documents from participating sites
  • Support study start-up, including regulatory documentation, essential documents, and IRB/IEC submissions
  • Prepare study-specific documents and materials
  • Keep study organizational charts and project trackers current
  • Conduct background checks for Principal Investigators
  • Set up Investigator Site Files and adapt study templates
  • Assign training documents in the Learning Management System and maintain the Project Team Training Matrix
  • Arrange and ship study materials and supplies to sites and Clinical Research Associates
  • Support Annual and Continuing Review IRB submissions in North America
  • Coordinate meetings and document minutes and follow-up actions
  • Arrange translations when needed
  • File, review, classify, name, and maintain documents in the electronic Trial Master File in line with the eTMF plan
  • Support scheduled TMF quality-control reconciliations and project close-out activities
  • Set up project email accounts and help organize email filing
  • Maintain strong working knowledge of Veeva Vault for eTMF administration and user support
  • Complete additional duties as assigned

Talablar

  • Associate degree or comparable professional experience
  • At least two years of experience in clinical research
  • Strong written and verbal communication skills with proficient English
  • Excellent interpersonal and communication abilities
  • Familiarity with ICH, GCP, FDA, MHRA, EMA, and applicable local guidelines
  • Proven ability to work effectively within a matrixed team
  • Consistent focus on quality and meticulous attention to detail
  • Ability to prioritize work and manage multiple responsibilities
  • Working knowledge of computer systems, software applications, and operating systems
  • Ability to sit for extended periods while working at a computer

Imtiyozlar

  • Paid time off
  • Comprehensive benefits package

O‘xshash ish o‘rinlari

Peraton

Senior Hybrid Connectivity Engineer

Peraton
H1B vizasi homiysiKonsaltingLogistikaSog‘liqni saqlash
USAmerika Qo‘shma ShtatlariVAVirjiniya
112 000 $ – 179 000 $ / yil
OfisdaTo‘liq stavkaO‘rta darajaSeniorTalab Qilinadigan Til: inglizchaMuhandis
AWSBulutDNSKiberxavfsizlikKubernetesTarmoqlararo ekranlarTCP/IPTypeScript

Designs and troubleshoots connectivity across AWS classified cloud, Kubernetes, and on-premises networks. Supports Peraton’s national security and government technology missions.

Ochish