Leading the development and continuous improvement of global pharmacovigilance signal detection processes, the full-time Associate Director Regulatory Affairs will ensure compliance with Health Authority requirements and serve as a subject matter expert while working remotely. Key responsibilities Oversee global pharmacovigilance signal detection and management processes Collaborate with cross-functional teams to maintain compliant processes and provide vendor oversight Develop and deliver training related to signal detection and management, while mentoring junior scientists Required qualifications Bachelor's degree in Life Sciences, Healthcare, Pharmacy, Medicine, or a related discipline Experience in pharmacovigilance and medical safety sciences Knowledge of EU pharmacovigilance regulations and regulatory inspection expectations Experience with signal detection methodologies and risk-benefit assessment Strong background in cross-functional collaboration within pharmaceutical or biotechnology organizations
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