Senior Clinical Research Associate
Worldwide Clinical Trials
full-time
Posted on:
Location Type: Remote
Location: Australia
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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
Requirements
- 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
- Health insurance
- Retirement plans
- Paid time off
- Flexible work arrangements
- Professional development
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 reporting
Soft Skills
managementcompliancecommunicationorganizational
Certifications
RNBSN