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Worldwide Clinical Trials
Worldwide Clinical Trials
1 001 – 5 000 Darbuotojai
H1B vizos rėmėjasKonsultavimasLogistikaSveikatos priežiūra
Worldwide Clinical Trials yra pasaulinė sutartinių klinikinių tyrimų organizacija, padedanti farmacijos ir biotechnologijų įmonėms viso vaistų kūrimo ciklo metu. Daugiau nei 30 metų patirtį turinti įmonė teikia klinikinės stebėsenos, duomenų valdymo, pacientų įdarbinimo ir reguliavimo konsultavimo paslaugas tokiose terapinėse srityse kaip onkologija, kardiologija ir retosios ligos. Jos požiūris derina plačią klinikinių tyrimų kompetenciją su individualia pagalba ir sudėtingiems tyrimams pritaikytais sprendimais.
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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.

ARArgentinaBRBrazilijaMXMeksikaNuotolinisVisas etatasJaunesnysis specialistasVidutinis lygisPrivaloma Kalba: anglųAsocijuotasis specialistasBendra
Google Cloud Platform

Aprašymas

  • 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

Reikalavimai

  • 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

Privalumai

  • 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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