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Senior Clinical Research Associate – Oncology
Worldwide Clinical TrialsClinical Research Associate managing oncology research projects at Worldwide Clinical Trials. Responsible for conducting research activities and ensuring compliance at participating sites with a focus on patient impact.
About the role
Key responsibilities & impact- 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
What you’ll need- 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
Comp & perks- Health insurance
- 401(k) matching
- Flexible work hours
- Paid time off
- Professional development opportunities
ATS Keywords
✓ Tailor your resumeApplicant 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