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ICON plc
ICON plc
LogistikaSvetovanjeZdravstveno varstvo
ICON plc je globalna pogodbena raziskovalna organizacija, ki zagotavlja storitve za zdravstveno in farmacevtsko industrijo. Njeno delo vključuje klinične, svetovalne in komercialne storitve, ki podpirajo razvoj zdravil od zgodnjih raziskav do dejavnosti po prihodu na trg. Podjetje ponuja rešitve, kot so decentralizirane klinične raziskave, ocenjevanje srčne varnosti, laboratorijske storitve za zgodnje klinične raziskave, medicinsko slikanje, regulatorne informacije in dokazi iz resničnega sveta. ICON plc ima tudi terapevtsko strokovno znanje na področjih, kot so bolezni srca in ožilja, onkologija, interna medicina, celične in genske terapije ter podobna biološka zdravila, pri čemer združuje analizo podatkov s pristopi, osredotočenimi na paciente, da pomaga napredovati klinične programe.
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Delovna mesta v podjetju

Clinical Trial Coordinator

Support ICON’s sponsor-dedicated clinical research operations by helping monitor U.S. trial sites remotely. Assist with trial documentation, compliance, site reporting, and team coordination.

USZdružene države AmerikeNa daljavoPolni delovni časSrednja ravenSeniorZahtevani Jezik: angleščinaKoordinator kliničnih preskušanjSplošno
Google Cloud Platform

Opis

  • Help monitor clinical trial sites for compliance with study protocols, regulations, and Good Clinical Practice (GCP) guidelines.
  • Prepare site documents, enter data, and track site performance measures.
  • Coordinate with cross-functional colleagues to share information and resolve site issues.
  • Keep site activity records accurate and help prepare monitoring reports.
  • Take part in training to build clinical trial management knowledge and skills.
  • Work with the team and stakeholders to deliver high-quality clinical research.

Zahteve

  • Hold a bachelor’s degree in a relevant area, such as life sciences, healthcare administration, or clinical research.
  • Experience in clinical research, site management, or a related administrative role is preferred but not required.
  • Have strong organizational skills and attention to detail, with the ability to manage several tasks effectively.
  • Knowledge of clinical trial processes and regulatory requirements is an advantage.
  • Bring strong communication and interpersonal skills and the ability to work well with a team.
  • Be willing to travel as needed, approximately 25% of the time.
  • Have legal authorization to work in the country where the role is based.

Ugodnosti

  • Base salary with performance-related incentives.
  • Health and wellbeing programs, including medical, dental, and vision coverage where applicable.
  • Retirement and pension plans.
  • Life assurance and disability coverage.
  • Employee assistance programs and wellbeing resources.
  • Structured training and career pathways for learning and development.

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