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Consulting Pharmacist – Quality and Pharmacovigilance
Ividata Life Sciences. Oversee the regulatory compliance of ICSR (Individual Case Safety Reports) .
About the role
Key responsibilities & impact- Oversee the regulatory compliance of ICSR (Individual Case Safety Reports)
- Monitor the timeliness of submissions to health authorities and partners
- Conduct root cause analyses in the event of delays
- Analyze compliance trends
- Implement corrective action plans
- Escalate identified issues
- Propose appropriate solutions
- Contribute to the continuous improvement of pharmacovigilance processes
- Meet the client’s critical submission timeline objectives
- Work across the pharmaceutical, biotechnology, medical device, animal health, cosmetics, and nutrition sectors
Requirements
What you’ll need- Pharmacy degree required
- 1–5 years of experience in pharmacovigilance and/or quality assurance
- Fluency in English is essential, including daily communication in English and work with scientific documentation
- Experience in an international or English-speaking environment is a plus
- Knowledge of international pharmacovigilance practices
- Proficiency in Quality Management Systems (QMS)
- Good understanding of the overall pharmacovigilance process landscape
Benefits
Comp & perks- Stimulating, collaborative, and continuously evolving environment
- High-impact assignments
- Work alongside passionate experts
- Contribute to the continuous improvement of pharmacovigilance processes
- Work across the entire product lifecycle
- Grow within a team of 160 consultants
- Opportunity to make a real impact through your ideas and expertise