Join BioScript Solutions as an Associate Manager in Pharmacovigilance Quality, where you will enhance safety reporting and compliance practices in a remote-friendly environment. This full-time position is based in the Greater Toronto Area.In this role, you will oversee and enhance the pharmacovigilance compliance framework, driving quality initiatives and monitoring key performance metrics. A minimum of 5 years experience in pharmacovigilance or a regulated healthcare workplace is required. You will also lead training development and address any deviations effectively.Key Responsibilities:Maintain compliance with safety reporting frameworksOversee quality reviews and monitoring metricsLead investigations into pharmacovigilance deviationsDevelop and manage training programs for team membersImplement process improvements in documentationRequirements:Bachelor's degree in Health Sciences or related field5+ years in pharmacovigilance or healthcareKnowledge of adverse event reporting requirementsExperience with quality assurance practicesAbility to manage training and guide staffElevate your expertise in pharmacovigilance quality with a team that values your contribution.#J-18808-Ljbffr

📌 Associate Manager In Pharmacovigilance Quality (Ottawa)
🏢 BioScript Solutions group
📍 Ottawa