Clinical Trial Operations Manager
4 days ago
- Draft, review, and ensure the quality of all documents related to Clinical Trial Application (CTA) dossiers in accordance with local and regional regulations.
- Provide regulatory review of core study documents to ensure compliance with regulatory standards.
- Perform quality control on CTA packages before submission to regulatory authorities.
VCLS offers a competitive salary package, estimated at around $110,000 per annum, based on industry benchmarks.
The successful candidate will work closely with our team to drive forward regulatory processes, ensuring compliance and contributing to innovative clinical trials. If you're passionate about regulatory science and possess the required skills and qualifications, we'd love to hear from you.
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