ICON plc
ICON plc
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.

Senior Clinical Research Associate (Canada, Remote)

Monitor clinical trials for ICON across investigative sites and remotely. Support protocol adherence and compliance with ICH-GCP, standard procedures, and applicable regulations.

Descriere

  • Track clinical study progress at investigative sites and through remote monitoring.
  • Verify that trials are conducted, documented, and reported in line with their protocols.
  • Check compliance with standard operating procedures, ICH-GCP, and applicable regulatory requirements.
  • Contribute to research for pharmaceutical, biotechnology, medical device, government, and public health organizations.

Cerințe

  • Hold a bachelor's degree or international equivalent in a scientific or health-related discipline, or have an equivalent combination of education and clinical research experience.
  • For a level 2 role, have at least one year of clinical monitoring experience or an equivalent combination of education and experience.
  • For a level 3 role, have at least three years of clinical monitoring experience.
  • Oncology monitoring experience is preferred.
  • Be able to travel up to 70%.
  • Know ICH requirements and local regulatory authority rules for drug trials.
  • Be legally authorized to work in the United States or Canada.
  • Not require employment visa sponsorship now or in the future.
  • Be bilingual in English and French.

Beneficii

  • Competitive base pay.
  • Incentives tied to performance.
  • Medical, dental, and vision coverage where offered.
  • Retirement and pension plans.
  • Life assurance and disability coverage.
  • Employee assistance programs and wellbeing resources.
  • Structured training and career development opportunities.
  • Supportive workplace policies and wellbeing initiatives.
  • Reasonable accommodations during recruitment.