Proven track record of demonstrated pharmacovigilance activities including processing and quality review of ICSRs. Experience in writing or contributing to aggregate reports, literature screening, reconciliation, and preparation of SOPs. Strong project management experience ideally from a service provider or CRO. Health care professional or life science graduate with relevant experience. Comfortable communicating at senior levels within pharmaceutical organizations. Good leadership qualities including planning, mentoring, meeting facilitation, communication, and problem-solving skills.