ClinChoice
Associate - Regulatory Affairs
- Remote
- Hybrid
- On-site
- Full-time
- Contract
... transformation of medicinal product data to meet IDMP standards. • Monitor updates and changes to EMA’s IDMP implementation guidelines and ensure adherence. • Provide data validation, quality control, and remediation as needed. • Support EU shift operations, including data entry, review, and regulatory reporting. • Coordinate with ...
Chennai, भारत