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Knowledge, Skills, and Abilities:
- Excellent analytical and problem-solving skills
- Excellent oral and written communication in English
- Knowledge of MedDRA, Oracle ARGUS, and online literature searching preferred
- Excellent organizational and interpersonal skills; experience in working in a dynamic team environment
- Excellent knowledge of relevant local and international regulations and ICH guidelines on safety data management in clinical trials and post-approval
- Advanced knowledge of Microsoft Office: Excel, PowerPoint, Word
Experience:
- Core PV experience of at least 2-3 years in the pharmaceutical industry
- Preferred experience of at least 1-2 years in periodic reviews on aggregate safety data
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