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 - Canada Remote

ICON plc is seeking a Senior Clinical Research Associate to monitor respiratory and cardiovascular trials across the Greater Toronto Area. The role oversees site performance, regulatory compliance, data quality, and trial delivery.

Apraksts

  • Manage clinical trial activities in line with study protocols, regulations, and industry standards
  • Direct technically complex monitoring activities while advancing quality and continuous improvement
  • Evaluate site compliance with protocols, regulations, and Good Clinical Practice (GCP) requirements
  • Conduct site visits to review performance, address issues, and support effective trial delivery
  • Partner with cross-functional teams to maintain accurate, timely data collection and reporting
  • Train and support site personnel and fellow Clinical Research Associates
  • Develop productive relationships with site teams and stakeholders to support efficient trial operations
  • Monitor respiratory and cardiovascular studies throughout the Greater Toronto Area

Prasības

  • Bachelor’s degree in a relevant scientific or healthcare-related discipline
  • Extensive Clinical Research Associate experience with a strong grasp of clinical trial processes and regulatory obligations
  • Demonstrated ability to oversee multiple sites and projects while applying strong organization and problem-solving skills
  • Advanced knowledge of monitoring methods, data integrity, and site management
  • Proficiency with relevant clinical trial software and tools
  • Strong communication, interpersonal, and stakeholder management capabilities, including the ability to influence compliance in complex settings
  • Availability to travel as needed, approximately 60%
  • Legal authorization to work in the country where the position is based

Priekšrocības

  • Base salary with performance-based incentives
  • Health and wellbeing programmes, including medical, dental, and vision coverage where applicable
  • Retirement and pension programmes
  • Life assurance and disability coverage
  • Employee assistance programmes and wellbeing resources
  • Structured training and career development opportunities

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