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

Coordinate clinical trial data and study records for ICON’s sponsor-dedicated pharmaceutical research programs. Maintain data quality, regulatory compliance, and on-time study delivery.

Opis

  • Plan and analyse clinical trials, interpreting complex medical data
  • Lead technically demanding clinical research tasks, promoting quality and ongoing improvement
  • Prepare and maintain data management plans and records in line with industry standards and regulatory requirements
  • Resolve data discrepancies and other issues to improve data flow and quality across the study lifecycle
  • Work with clinical operations, biostatistics, and other teams to shape and carry out study-specific data management strategies
  • File and archive study records and send queries to investigator sites as part of project work
  • Guide junior coordinators in data reconciliation, coding, and cleaning
  • Keep study activities on schedule

Zahteve

  • Bachelor’s degree in a relevant discipline, such as life sciences or healthcare
  • Demonstrated clinical data management experience in the pharmaceutical or biotechnology sector
  • Familiarity with data management platforms such as Medidata, Oracle RDC, or comparable systems
  • Strong attention to detail and effectiveness in a fast-paced setting
  • Clear communication skills and ability to work across teams
  • Knowledge of regulatory guidance and standards such as ICH-GCP is an advantage
  • Availability to travel when needed, approximately 5%
  • Legal authorization to work in the country where the position 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 insurance and disability coverage
  • Employee assistance programs and wellbeing resources
  • Training and career development through structured learning opportunities

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