Join BioScript Solutions as an Associate Manager in Pharmacovigilance Quality, where you will enhance safety reporting and compliance practices in a remote-friendly setting. 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 environment is required. You will also lead training development and address any deviations effectively. Key Responsibilities:

- Maintain compliance with safety reporting frameworks
- Oversee quality reviews and monitoring metrics
- Lead investigations into pharmacovigilance deviations
- Develop and manage training programs for team members
- Implement process improvements in documentation Requirements:
- Bachelor's degree in Health Sciences or related field
- 5+ years in pharmacovigilance or healthcare
- Knowledge of adverse event reporting requirements
- Experience with quality assurance practices
- Ability to manage training and guide staff Elevate your expertise in pharmacovigilance quality with a team that values your contribution.

📌 Associate Manager in Pharmacovigilance Quality (Canada)
🏢 BioScript Solutions group
📍 Canada