Senior Clinical Research Associate – Lead CRA
IQVIA
full-time
Posted on:
Location Type: Office
Location: Ho Chi Minh • Vietnam
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Job Level
About the role
- Oversee study monitoring plan compliance for assigned studies
- Serve as the primary point of contact for IQVIA CRAs
- Provide oversight of site monitoring data management activities
- Review Monitoring Visit Reports and provide guidance
- Prepare and lead regular meetings with IQVIA CRA and sponsor Project Manager
- Collaborate and liaise with sponsor Project Manager for project execution support
- Support CRA with study issue resolution
Requirements
- More than 4 years of onsite monitoring experience
- Experience in site monitoring data management activities
- Familiarity with study monitoring plan compliance
- Strong ability to collaborate with Project Managers
- Ability to lead and follow up on regular meetings
- Proficiency in reviewing Monitoring Visit Reports
- Skills in resolving study-related questions
Benefits
- Professional development opportunities
- Remote work options
Applicant Tracking System Keywords
Tip: use these terms in your resume and cover letter to boost ATS matches.
Hard Skills & Tools
onsite monitoring experiencesite monitoring data managementstudy monitoring plan compliancereviewing Monitoring Visit Reportsstudy issue resolution
Soft Skills
collaborationleadershipcommunicationproblem-solvingmeeting facilitation