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 – Quebec Remote | ICON plc

Monitor cardiovascular and respiratory clinical trials across Quebec for ICON plc, supporting site compliance, data quality, and adherence to study protocols.

Apraksts

  • Manage clinical trial activities in line with study protocols, regulations, and industry standards
  • Lead monitoring work with an emphasis on quality and ongoing process improvement
  • Evaluate site compliance with protocols, regulations, and Good Clinical Practice requirements
  • Perform site visits to review performance, address issues, and support effective study delivery
  • Work with cross-functional teams to coordinate accurate, timely data collection and reporting
  • Train and advise site personnel and fellow Clinical Research Associates
  • Develop and sustain effective working relationships with site teams and study stakeholders
  • Monitor cardiovascular and respiratory studies conducted in Quebec

Prasības

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

Priekšrocības

  • Base salary with performance-based incentives
  • Health and wellness programs, including medical, dental, and vision coverage where applicable
  • Retirement and pension programs
  • Life insurance and disability protection
  • Employee assistance programs and wellbeing support resources
  • Professional development through structured training and career progression pathways

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