Demonstrates expertise in clinical monitoring, ensuring compliance with ICH-GCP and regulatory requirements while effectively supporting clinical research across various sectors. Proficient in managing clinical trials and capable of traveling as needed to oversee study progress.

Highest-signal resume keywords

Clinical Monitoring ExperienceKnowledge Of ICH-GCPOncology Monitoring ExperienceBilingual English/FrenchBachelor's Degree In Scientific Or Health-Related Field

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 in accordance with the protocol
Follow standard operating procedures (SOPs), ICH-GCP, and applicable regulatory requirements
Support clinical research for pharmaceutical, biotechnology, medical device, government, and public health organizations
Travel up to 70%

Requirements

What you’ll need

Bachelor's degree, or its international equivalent in a scientific or health-related field, or an equivalent combination of education and clinical research 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
Employment contingent upon having the legal right to work in the country where the role is based

Benefits

Comp & perks

Competitive base salary and performance related incentives
Health and wellbeing programmes including medical, dental, and vision coverage where applicable
Retirement and pension plans
Life assurance and disability coverage
Employee assistance programmes and wellbeing resources
Learning and development opportunities through structured training and career pathways
Comprehensive and competitive total reward package
Supportive policies and wellbeing initiatives
Continuous learning culture and professional development opportunities
Equal opportunity and inclusive workplace
Reasonable accommodation during the recruitment process
Benefits may vary depending on role and location

ATS Keywords

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Applicant Tracking System Keywords

Tip: use these terms in your resume and cover letter to boost ATS matches.

Hard Skills

Clinical Trial ManagementRegulatory ComplianceData Recording And ReportingStandard Operating Procedures (SOPs)Clinical Research Methodologies

Industry Keywords

Pharmaceutical ResearchBiotechnologyMedical Device TrialsPublic Health OrganizationsInvestigative Sites