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Job Description
Senior Regulatory Affairs Specialist job description: Manage regulatory activities, develop strategies, and submit to global agencies. Key responsibilities include preparing high-quality CMC submissions, contributing to regulatory strategies, and collaborating with stakeholders. The ideal candidate has 3-5 years of experience in a Pharmaceutical company, a Bachelor's/Graduate degree in a relevant science discipline, and excellent written, oral communication, and project management skills. Required core competencies include action-oriented, detail-focused, and results-driven individuals with strong leadership, interpersonal, and presentation skills.