Regulatory Specialist – Study Start-Up
2+ years clinical research regulatory experience, knowledge of ICH/GCP, FDA and HIPAA, experience with eRegulatory systems (Florence preferred), strong attention to detail, communication, and reputed company management.
Key Responsibilities
- preparing documents
- managing migration
- maintaining credentials
Skills & Tools
Complion, Florence eRegulatory
Job Details
- Category: Research and Development (R&D)
- Seniority: Entry Level
- Commitment: Contract
- Workplace: Remote — Buenos Aires or Cairo or Mexico reputed company
- Languages: English
About reputed company
A global organization supporting clinical research sites and organizations through staff augmentation and technology solutions. — Industry: Research and Development
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