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Worldwide Clinical Trials
Worldwide Clinical Trials
1001 – 5000 Darbinieki
H1B vīzas sponsorsKonsultācijasLoģistikaVeselības aprūpe
Worldwide Clinical Trials ir globāla līgumizpētes organizācija, kas atbalsta farmācijas un biotehnoloģiju uzņēmumus visā zāļu izstrādes ciklā. Ar vairāk nekā 30 gadu pieredzi uzņēmums nodrošina klīnisko pētījumu uzraudzību, datu pārvaldību, pacientu piesaisti un konsultācijas regulējuma jautājumos tādās terapeitiskajās jomās kā onkoloģija, kardioloģija un retās slimības. Tā pieeja apvieno plašu klīnisko pētījumu pieredzi ar personalizētu atbalstu un sarežģītiem pētījumiem pielāgotiem risinājumiem.
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Vakances uzņēmumā

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.

ARArgentīnaBRBrazīlijaMXMeksikaAttālinātiPilna slodzeJaunākais speciālistsVidējais līmenisNepieciešamā Valoda: angļuAsociētais speciālistsVispārīgi
Google Cloud Platform

Apraksts

  • 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

Prasības

  • 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

Priekšrocības

  • 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

Saistītās vakances

ICON plc

Clinical Data Coordinator – Argentina (Remote)

ICON plc
KonsultācijasLoģistikaVeselības aprūpe
ARArgentīnaAttālinātiPilna slodzeVidējais līmenisVecākais speciālistsNepieciešamā Valoda: angļuKlīnisko datu koordinatorsVispārīgi
Google Cloud PlatformOracle

Support clinical trial data management at ICON Strategic Solutions by reviewing study data and raising queries with research sites. Help deliver sponsor-dedicated studies and keep project activities on schedule.

Atvērt