Initiation Clinical Research Associate I
Parexel(1 day ago)
About this role
This role focuses on managing the start-up and maintenance phases of clinical trial sites, ensuring regulatory compliance and high-quality documentation, and fostering strong relationships with investigators and site staff. The individual supports the overall progress of clinical studies from site identification to close-out, working independently and proactively to meet project goals.
Required Skills
- Regulatory Compliance
- Clinical Trials
- Project Management
- GCP
- Clinical Documentation
- Stakeholder Management
- Regulatory Submissions
- Quality Assurance
- Investigator Relations
- CTMS
About Parexel
parexel.comFor over 35 years Parexel has been a trusted global CRO and biopharmaceutical services company. Learn more about how we can help.
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