ICON plc
ICON plc
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.

Senior Clinical Data Coordinator, Standards

Senior coordinator overseeing clinical trial data and standards for ICON’s sponsor-dedicated research programs. Supports data quality, compliance, reconciliation, and timely study delivery.

Opis

  • Plan and assess clinical trials, interpret complex medical data, and support the development of new treatments and therapies.
  • Lead technically demanding clinical research activities, prioritizing quality and ongoing improvement.
  • Develop and maintain data management plans and study records in line with industry standards and regulatory requirements.
  • Find and resolve data inconsistencies to improve data flow and quality across the study lifecycle.
  • Work with clinical operations and biostatistics teams to design and carry out study-specific data management approaches.
  • Complete project work to keep studies on schedule, including filing and archiving records and sending queries to investigator sites.
  • Guide junior data coordinators in data reconciliation, coding, and cleaning practices.

Zahteve

  • Bachelor’s degree in a relevant discipline, such as life sciences or healthcare.
  • Demonstrated clinical data management experience in the pharmaceutical or biotechnology industry.
  • Familiarity with clinical data management tools such as Medidata, Oracle RDC, or similar systems.
  • Strong attention to detail and effectiveness in a fast-paced work environment.
  • Excellent communication and ability to work with cross-functional teams.
  • Knowledge of regulatory guidance and standards, such as ICH-GCP, is an advantage.
  • Willingness to travel as needed, approximately 5%.
  • Must have legal authorization to work in the country where the role is based; employment with ICON is conditional on this.

Ugodnosti

  • Competitive base pay and performance-based incentives.
  • Health and wellbeing programs, including medical, dental, and vision coverage where applicable.
  • Retirement and pension plans.
  • Life insurance and disability coverage.
  • Employee assistance programs and wellbeing resources.
  • Learning and development through structured training and career pathways.

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