Clinical Research Associate, Bilingual – Oncology
Worldwide Clinical Trials
full-time
Posted on:
Location Type: Remote
Location: Canada
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About the role
- Responsible for managing research activities at clinical research project sites
- Conduct study initiation visits (SIVs)
- Ensure compliance with obtaining informed consent and adhering to regulatory requirements
Requirements
- 2+ years of experience as a Clinical Research Associate
- 4-year university degree OR Nursing Degree
- Experience in Oncology is required
- Bilingual (English/French) is required
- Candidates must reside in Eastern Canada
- Proficiency in Microsoft Office, CTMS, and EDC Systems
Benefits
- Supportive and team-oriented environment
- Professional development opportunities
- Clear career path to Clinical Trial Manager roles
- Accessible Executive Leadership team
Applicant Tracking System Keywords
Tip: use these terms in your resume and cover letter to boost ATS matches.
Hard Skills & Tools
clinical researchinformed consentregulatory compliancestudy initiation visitsOncology
Soft Skills
bilingualcommunication
Certifications
4-year university degreeNursing Degree