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ICON plc
ICON plc
Asistență medicalăConsultanțăLogistică
ICON plc este o organizație globală de cercetare în regim contractual, care deservește industriile din domeniul sănătății și farmaceutic. Activitatea sa cuprinde servicii clinice, de consultanță și comerciale care sprijină dezvoltarea medicamentelor, de la cercetarea timpurie până la activitățile post-comercializare. Compania oferă soluții precum studii clinice descentralizate, evaluarea siguranței cardiace, laboratoare clinice pentru etapele timpurii, imagistică medicală, informații de reglementare și dovezi din lumea reală. ICON plc dispune, de asemenea, de expertiză terapeutică în domenii precum bolile cardiovasculare, oncologia, medicina internă, terapiile celulare și genice și medicamentele biosimilare, combinând analiza datelor cu o abordare axată pe pacienți pentru a contribui la avansarea programelor clinice.
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Clinical Research Associate – Canada Remote | ICON plc

Monitor respiratory and cardiovascular clinical trials for ICON Strategic Solutions across Canada's Greater Toronto Area. Coordinate site visits, compliance, data quality, and guidance for clinical research teams.

CACanadaRemoteNormă întreagăJuniorNivel mediuLimbă Obligatorie: englezăCercetare clinică
Google Cloud Platform

Descriere

  • Manage clinical trial activities in line with study protocols, regulations, and industry standards
  • Drive monitoring activities focused on quality and ongoing process improvement
  • Evaluate site compliance with protocols, regulations, and Good Clinical Practice requirements
  • Complete site visits to review performance, address issues, and support effective study delivery
  • Partner with cross-functional teams to ensure accurate, timely data collection and reporting
  • Train and advise site staff and fellow Clinical Research Associates
  • Develop and sustain productive relationships with site teams and other stakeholders
  • Monitor respiratory and cardiovascular studies throughout the Greater Toronto Area

Cerințe

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

Beneficii

  • Competitive base pay with performance-based incentives
  • Health and wellness programs, including medical, dental, and vision coverage where available
  • Retirement and pension provisions
  • Life insurance and disability protection
  • Employee assistance programs and wellbeing resources
  • Structured training, professional development, and career progression opportunities

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