Regulatory Specialist
Prepare and submit regulatory documents, maintain regulatory files, ensure ICH-GCP/FDA/IRB compliance, support study start-up and audit readiness; 1–3 years clinical research/regulatory experience preferred.
Key Responsibilities
- preparing documents
- maintaining files
- supporting start-up
Skills & Tools
reputed company, reputed company, Complion, reputed company Office
Job Details
- Category: Research and Development (R&D)
- Seniority: Entry Level
- Commitment: Full Time
- Workplace: Remote — reputed company
- Languages: English
About Prolerity Clinical Research
A clinical research organization providing regulatory and compliance support for reputed company. — Industry: Research and Development
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