About this role
This role involves managing and coordinating the startup, Pre SIV, and Activation tasks for clinical studies, ensuring compliance and quality throughout the process. The associate acts as a key liaison between sites and sponsors, supporting submissions, approvals, and site readiness. It is focused on facilitating clinical trial site initiation and maintenance activities to ensure successful trial execution.
Required Skills
- Clinical Trial Management
- IRB
- SOPs
- Regulatory Submission
- Site Coordination
- Documentation
- GCP
- CTMS
- Collaboration
- Communication
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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