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 Research Associate, Remote Oncology Trials

Lead remote monitoring for Phase I oncology trials with ICON Strategic Solutions. Oversee sites, compliance, data quality, and CRA support.

Apraksts

  • Direct clinical trial activities in line with protocols, regulations, and industry standards
  • Lead technically complex monitoring work with an emphasis on quality and ongoing improvement
  • Verify site compliance with study protocols, regulations, and Good Clinical Practice standards
  • Conduct site visits, evaluate performance, resolve issues, and support effective study delivery
  • Coordinate with cross-functional teams to ensure accurate, timely data collection and reporting
  • Train and mentor site staff and fellow Clinical Research Associates
  • Develop and sustain effective relationships with site teams and key stakeholders

Prasības

  • Bachelor’s degree in a relevant scientific or healthcare-related discipline
  • Extensive Clinical Research Associate experience with strong knowledge of clinical trial processes and regulatory requirements
  • Demonstrated ability to manage multiple sites and projects while applying strong organization and problem-solving skills
  • Advanced knowledge of monitoring practices, data integrity, and site management, including relevant clinical trial software and tools
  • Strong communication, interpersonal, and stakeholder management abilities, with the capacity to promote compliance in complex environments
  • Willingness to travel approximately 60% as required
  • Current oncology monitoring experience
  • Legal authorization to work in the country where the role is based

Priekšrocības

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

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