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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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Locurile de muncă ale companiei

Clinical Research Associate – Canada Remote

Monitor sponsor-dedicated clinical trials for ICON, a global clinical research organization. Support protocol compliance, reliable data, and patient safety across Canadian trial sites.

CACanada
89.728 $ – 112.160 $ / an
RemoteNormă întreagăJuniorNivel mediuLimbă Obligatorie: englezăCercetare clinică
Google Cloud Platform

Descriere

  • Manage site qualification, initiation, monitoring, and close-out visits for clinical trials.
  • Maintain protocol compliance, data integrity, and patient safety throughout each study.
  • Partner with investigators and site teams to support efficient study execution.
  • Review clinical data and resolve queries to uphold data quality.
  • Help prepare and review study materials, including protocols and clinical study reports.
  • Support clinical trial design and analysis, interpret complex medical data, and contribute to the development of new treatments.
  • Own assigned deliverables while working collaboratively within a sponsor-dedicated model.

Cerințe

  • Bachelor’s degree in a scientific or healthcare-related discipline.
  • At least two years of Clinical Research Associate experience.
  • Detailed understanding of clinical trial operations, applicable regulations, and ICH-GCP guidelines.
  • Strong organizational and communication abilities with careful attention to detail.
  • Capacity to work independently and collaboratively in a fast-paced setting.
  • Availability to travel as needed, approximately 60% of the time.
  • Legal authorization to work in the country where the position is located.

Beneficii

  • Competitive base pay with performance-based incentives.
  • Health and wellness programs, including medical, dental, and vision coverage where applicable.
  • Retirement and pension plans.
  • Life insurance and disability coverage.
  • Employee assistance programs and wellness resources.
  • Professional development through structured training and career pathways.

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