ICON plc
ICON plc
ICON plc ir globāla līgumizpētes organizācija, kas apkalpo veselības aprūpes un farmācijas nozares. Tās darbība ietver klīniskos, konsultāciju un komerciālos pakalpojumus, kas atbalsta zāļu izstrādi no agrīnas izpētes līdz darbībām pēc zāļu nonākšanas tirgū. Uzņēmums piedāvā decentralizētus klīniskos pētījumus, sirds drošuma novērtēšanu, agrīnās klīniskās laboratorijas pakalpojumus, medicīnisko attēlveidošanu, regulatīvo informāciju un reālās pasaules pierādījumu risinājumus. ICON plc ir arī terapeitiskā kompetence tādās jomās kā sirds un asinsvadu slimības, onkoloģija, iekšķīgās slimības, šūnu un gēnu terapijas, kā arī bioloģiski līdzīgas zāles. Apvienojot datu analīzi ar uz pacientu vērstām pieejām, uzņēmums palīdz attīstīt klīniskās programmas.

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.

Apraksts

  • 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

Prasības

  • 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

Priekšrocības

  • 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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