Senior Clinical Research Associate – Oncology
Worldwide Clinical Trials
full-time
Posted on:
Location Type: Remote
Location: Canada
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Job Level
About the role
- Responsible for managing the research activities at sites participating in Worldwide’s clinical research projects
- Conduct study initiation visits (SIVs)
- Ensure compliance with obtaining informed consent and reporting potential safety-related events
- Adhere to all applicable regulatory requirements
Requirements
- 5+ years of experience as a Clinical Research Associate
- 4-year university degree OR Nursing Degree
- Experience in Oncology is required
- Fluent in written and verbal English and French is required
- Candidates must reside in Canada
- Willingness to travel regionally required
Benefits
- Health insurance
- 401(k) matching
- Flexible work hours
- Paid time off
- Professional development opportunities
Applicant Tracking System Keywords
Tip: use these terms in your resume and cover letter to boost ATS matches.
Hard Skills & Tools
clinical researchstudy initiation visitsinformed consentsafety reportingregulatory complianceOncology
Soft Skills
communicationinterpersonal skillsorganizational skillswillingness to travel
Certifications
4-year university degreeNursing Degree