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Senior Clinical Research Associate
Worldwide Clinical TrialsClinical Research Associate responsible for managing research activities in clinical trials across Australia. Overseeing site management and ensuring compliance with regulatory standards.
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
Requirements
What you’ll need- 5+ years of experience as a Clinical Research Associate
- 4-year university degree or RN/BSN in Nursing
- Proficiency in Microsoft Office, CTMS and EDC Systems
- Willingness to travel
Benefits
Comp & perks- Health insurance
- Retirement plans
- Paid time off
- Flexible work arrangements
- Professional development
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 reporting
Soft Skills
managementcompliancecommunicationorganizational
Certifications
RNBSN