Medical Advisor
Core
Evaluate clinical trial data and scientific information to determine if medicine benefits outweigh risks, and regulate medicines in use.
Role type
Senior IC medical advisor (pharmacovigilance and regulatory)
Builds
Regulatory decisions on new medicines and indications for New Zealanders
Domain
Healthcare regulation / Pharmacovigilance
Required skills
Medical qualification, critical appraisal of clinical data, regulatory decision-making, safety monitoring, mentorship
Preferred skills
Ability to communicate complex clinical ideas to diverse groups, manage dynamic workload
Technologies
Clinical trial data systems, pharmacovigilance reporting tools
Responsibilities
Evaluate efficacy and safety of new and existing medicines; Present clinical evidence to expert advisory committees; Identify and address potential risks in medicine applications; Monitor and evaluate medicine safety performance; Mentor colleagues and review communications
Seniority
Senior, hands-on IC