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 – California Remote

Lead Phase I oncology trial monitoring for ICON’s sponsor-dedicated research programs. Oversee sites, compliance, data integrity, and clinical research associate guidance.

Apraksts

  • Manage clinical trial activities in line with protocols, regulations, and industry standards
  • Lead technically complex monitoring work focused on quality and continuous improvement
  • Assess site compliance with study protocols, regulations, and Good Clinical Practice standards
  • Conduct site visits to evaluate performance, resolve issues, and support trial delivery
  • Partner with cross-functional teams to ensure accurate, timely data collection and reporting
  • Train and support site staff and other clinical research associates
  • Maintain effective working relationships with site personnel and study 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 organizational and problem-solving skills
  • Advanced knowledge of monitoring practices, data integrity, and site management, including relevant clinical trial software and tools
  • Excellent communication, interpersonal, and stakeholder management abilities, with the capacity to influence 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 programs, including medical, dental, and vision coverage where applicable
  • Retirement and pension plans
  • Life assurance and disability coverage
  • Employee assistance programs and wellbeing resources
  • Structured training and career development opportunities

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