Senior Clinical Research Associate, Oncology
Parexel
full-time
Posted on:
Location Type: Remote
Location: United States
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Job Level
Tech Stack
About the role
- Responsible for the delivery of studies at allocated sites
- Collaborate with other CRAs and Local Study Team
- Ensure compliance with Client Procedural Documents and international guidelines
- Prepare, initiate, monitor, and close assigned sites in clinical studies
- Conduct monitoring visits and ensure accurate data management
Requirements
- 3+ years of direct Monitoring / CRA experience in a CRO or Pharma organization
- 2+ years direct Oncology Monitoring / CRA experience in a CRO or Pharma organization
- Excellent knowledge of international guidelines ICH-GCP
- Good knowledge of relevant local regulations
- Bachelor’s degree required
Benefits
- Health insurance
- 401(k) matching
- Paid time off
- Training and development opportunities
- Remote work flexibility
Applicant Tracking System Keywords
Tip: use these terms in your resume and cover letter to boost ATS matches.
Hard Skills & Tools
MonitoringClinical Research Associate (CRA)Data Management
Soft Skills
CollaborationCompliance