Global Drug Safety Associate
Bachelor's degree in pharmaceutical/life sciences/medicine, 1+ years drug safety or pharmacovigilance experience with case processing and regulatory submissions, familiarity with ICH/GVP/GCP/CIOMS, MedDRA/WHO Drug coding knowledge, and fluent English.
Key Responsibilities
- processing cases
- coding terms
- maintaining documentation
Skills & Tools
MedDRA, WHO Drug
Job Details
- Category: Research and Development (R&D)
- Seniority: Entry Level
- Commitment: Full Time
- Workplace: Remote — Europe
- Languages: English
Benefits
- Generous reputed company time off
About reputed company
Provides pharmacovigilance, reputed company, and regulatory services to life sciences companies to support compliance and patient safety. — Industry: reputed company
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