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Worldwide Clinical Trials
Worldwide Clinical Trials
1 001 – 5 000 Xodimlar
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Worldwide Clinical Trials farmatsevtika va biotexnologiya kompaniyalarini dori vositalarini ishlab chiqish jarayonining barcha bosqichlarida qo‘llab-quvvatlaydigan global shartnoma asosidagi tadqiqot tashkilotidir. 30 yildan ortiq tajribaga ega kompaniya onkologiya, kardiologiya va noyob kasalliklar kabi turli terapevtik yo‘nalishlarda klinik monitoring, ma’lumotlarni boshqarish, bemorlarni jalb qilish va tartibga solish bo‘yicha konsalting xizmatlarini taqdim etadi. Uning yondashuvi keng qamrovli klinik tadqiqotlar tajribasini murakkab tadqiqotlar uchun shaxsiylashtirilgan yordam va moslashtirilgan yechimlar bilan birlashtiradi.
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Remote Clinical Trials Associate in Argentina

Support documentation, system access, training, and project tracking for Worldwide Clinical Trials’ global research projects. Remote role serving Argentina, Mexico, and Brazil.

ARArgentinaBRBraziliyaMXMeksikaMasofaviyTo‘liq stavkaJuniorO‘rta darajaTalab Qilinadigan Til: inglizchaAssotsiatsiyalangan mutaxassisUmumiy
Google Cloud Platform

Tavsif

  • Help clinical project teams with administrative tasks and project tracking
  • Manage system access requests for Project Managers, Lead CRAs, and CRAs, and monitor their progress
  • Keep project portals up to date and check document versions for accuracy
  • Assist with preparing, shipping, version-controlling, and filing trial records, including Investigator Site Files and Trial Master File documents
  • Maintain project records, such as site medical question-and-answer logs and details about participating sites and staff
  • Prepare and share minutes from sponsor, project, and internal management meetings
  • Organize and monitor training specific to each project
  • Carry out administrative tasks accurately and on time to support effective clinical trial delivery
  • Work across time zones with Project Managers, Lead CRAs, CRAs, and colleagues around the world

Talablar

  • A degree or equivalent experience
  • At least one year of experience in a related role
  • Strong written and spoken English
  • Fluency in the language of the country where the role is based
  • Knowledge of ICH, GCP, and applicable FDA or EU directive regulations
  • Strong organizational, problem-solving, and interpersonal abilities
  • Excellent attention to detail and quality
  • Ability to work independently and collaboratively
  • Ability to manage competing priorities, use independent judgment, and adapt in a fast-changing environment
  • Excellent command of Microsoft Office, including Outlook, Word, Excel, and PowerPoint

Imtiyozlar

  • A collaborative, inclusive workplace
  • Opportunities for career growth and development
  • Opportunities to learn and grow
  • Meaningful work that helps improve patients’ lives through clinical research

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