- Good medical and pharmacovigilance (PV) knowledge to guide and train the team on related medical content, besides being able to detect adverse events in qualitative data using medical knowledge
- Basic knowledge and understanding of the global pharma industry
- Awareness of the various regulatory guidelines involved in PV
- Quick decision-making skills (e.g., classification into doubtful adverse event vs. AE vs. serious AE, or no AE)
- Excellent (verbal/written) communication and interpersonal skills
- Great eye for detail for flawless execution and QC review
- Demonstrated project management skills and time management skills to deliver projects on time or ahead of schedule
- MS Office - PowerPoint, Excel, and Word
- Drive for excellence and passion for quality, with the ability to adapt to international culture (applicable in analyzing slang and colloquial terminology)
- Ability and passion for continuous learning
- Inclination and interest to learn more about adverse event reporting / Pharmacovigilance
- Excellent problem solving skills
Strongly desirable competencies:
