Catalogue update: this role is no longer listed in the current micro1 catalogue. Browse current AI Training opportunities.
About the role
Bring your medicine experience to this Pharmacovigilance Expert opportunity.
Skills and focus areas
pharmacovigilance · drug safety report authoring · dsur/psur/pbrer review · ich e2f and ich e2c(r2) compliance · gvp guidelines · aggregate safety data analysis · signal management · benefit-risk assessment · meddra coding · seriousness and causality assessment · expectedness determination · data reconciliation · regulatory documentation · structured written communication · attention to detail
What you will do
- Construct realistic assessment problems grounded in professional practice.
- Build or assess financial analyses, checking assumptions and the business implications.
- Review accounting work and financial records for consistency and supportable conclusions.
- Check technical or professional work against the relevant compliance constraints.
Experience and requirements
- Relevant areas of expertise: pharmacovigilance, drug safety report authoring, dsur/psur/pbrer review, ich e2f and ich e2c(r2) compliance.
- The client specifies: “5+ years of pharmacovigilance or drug safety experience at a sponsor, CRO, or as an independent consultant.”
Working arrangements
- The engagement is offered on a contractor basis.
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