LogoFresh Jobs Ahead
ICON plc
ICON plc
ConsultingHealthcareLogistics
ICON plc is a global contract research organisation serving the healthcare and pharmaceutical industries. Its work spans clinical, consulting, and commercial services that support drug development from early research through post-marketing activities. The company provides solutions including decentralised clinical trials, cardiac safety, early clinical laboratories, medical imaging, regulatory intelligence, and real-world evidence. ICON plc also brings therapeutic expertise to areas such as cardiovascular disease, oncology, internal medicine, cell and gene therapies, and biosimilars, combining data analysis with patient-focused approaches to help advance clinical programmes.
LinkedIn
Company Jobs

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.

CACanadaUSUnited States
$108,576 – $135,720 / year
RemoteFull-timeSeniorEnglish RequiredFrench RequiredClinical Research
Google Cloud Platform

Description

  • 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.

Requirements

  • 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.

Benefits

  • 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.

Related Jobs