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Worldwide Clinical Trials
Worldwide Clinical Trials
1001 – 5000 Zaposleni
Sponzor vizuma H1BLogistikaSvetovanjeZdravstveno varstvo
Worldwide Clinical Trials je globalna pogodbena raziskovalna organizacija, ki farmacevtskim in biotehnološkim podjetjem pomaga v celotnem življenjskem ciklu razvoja zdravil. Podjetje ima več kot 30 let izkušenj ter zagotavlja klinično spremljanje, upravljanje podatkov, pridobivanje bolnikov in regulativno svetovanje na terapevtskih področjih, vključno z onkologijo, kardiologijo in redkimi boleznimi. Njegov pristop združuje široko strokovno znanje o kliničnih preskušanjih s prilagojeno podporo in rešitvami, oblikovanimi za kompleksne študije.
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Delovna mesta v podjetju

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.

ARArgentinaBRBrazilijaMXMehikaNa daljavoPolni delovni časJuniorSrednja ravenZahtevani Jezik: angleščinaSodelavecSplošno
Google Cloud Platform

Opis

  • 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

Zahteve

  • 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

Ugodnosti

  • 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

Sorodna delovna mesta