Senior Clinical Research Associate

ICON plc

. Monitor the progress of clinical studies at investigative sites or remotely .

Posted 10/7/2026full-timeRemote • Canada, United StatesSeniorWebsite

Core Competencies

Role fit

Core Competencies

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Demonstrates expertise in clinical monitoring, ensuring compliance with ICH-GCP and regulatory requirements while supporting the development of medicines and medical devices. Proficient in conducting clinical trials and monitoring activities, with a strong focus on oncology.

Highest-signal resume keywords

Clinical Monitoring ExperienceOncology Monitoring ExperienceKnowledge of ICH-GCPBilingual English/FrenchBachelor's Degree in Scientific Field

ATS Keywords

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Applicant Tracking System Keywords

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Hard Skills

Clinical MonitoringRegulatory ComplianceClinical Trial ManagementData ReportingSOP AdherenceStudy Protocol ComplianceClinical Research ExperienceOncology KnowledgeTravel FlexibilityHealthcare Professional Qualification

Industry Keywords

ICH GuidelinesClinical StudiesInvestigative SitesOutsourced Clinical ResearchDrug TrialsRegulatory Authority RegulationsHealth-Related FieldScientific FieldBilingual CommunicationTravel Requirements

About the role

Key responsibilities & impact

Monitor the progress of clinical studies at investigative sites or remotely
Ensure clinical trials are conducted, recorded, and reported according to the protocol
Ensure compliance with standard operating procedures (SOPs), ICH-GCP, and applicable regulatory requirements
Conduct clinical monitoring activities in study sites or remotely
Support the development of medicines and medical devices through outsourced clinical research services

Requirements

What you’ll need

Bachelor's degree or international equivalent in a scientific or health-related field, or equivalent combination of education and clinical research experience
Alternatively, authorized healthcare professional qualification such as registered nurse, or equivalent work experience
1+ years of clinical monitoring experience or equivalent combination of education and experience for the level 2 role
3+ years of clinical monitoring experience for a level 3 role
Oncology monitoring experience preferred
Ability to travel 70%
Knowledge of ICH and local regulatory authority regulations regarding drug trials
Legally authorized to work in the United States or Canada
Must not require now or in the future sponsorship for employment visa status
Bilingual English/French required

Benefits

Comp & perks

Continuous learning culture and professional development opportunities
Competitive base salary
Variable pay and recognition programs
Employee benefits including health and wellbeing programmes, medical, dental, and vision coverage where applicable
Retirement and pension plans
Life assurance and disability coverage
Employee assistance programmes and wellbeing resources
Structured training and career pathways
Supportive policies and wellbeing initiatives
Reasonable accommodations during the recruitment process
Equal opportunity and inclusive workplace