Pharmacovigilance Services Associate Manager

Role Overview As a Pharmacovigilance Services Associate Manager, you will be responsible for conducting comprehensive medical reviews of aggregate and RMP reports within strict timeframes while maintaining the highest standards of accuracy. This role involves ensuring compliance with client standard operating procedures and global regulatory requirements to protect patient safety and maintain the efficacy of pharmaceutical products. Key Responsibilities - Conduct medical review of aggregate and RMP reports ensuring accuracy, completeness and consistency in compliance with SOPs and regulatory requirements - Manage and develop individual case narratives describing adverse events for inclusion in regulatory submissions and safety reports - Address all previous health authority comments and provide medical analysis for relevant report sections - Perform quality control of assigned aggregate reports and RMP documents while managing medical queries from clients - Participate in knowledge management meetings, project planning and strategy discussions to align deliverables with client objectives - Provide coaching, review feedback and knowledge sharing to mentees on medically analyzed reports - Notify critical deviations to the Quality Management team within one business day and minor deviations within three business days Required Qualifications - MBBS or MD degree - 3 to 14 years of experience in pharmacovigilance - Medical review experience in adverse reaction reports, risk management plans and signal management - Expert level proficiency in English - Strong understanding of global regulatory requirements and compliance standards Why Join Us Accenture offers opportunities to work on challenging healthcare projects while contributing to pharmaceutical safety initiatives that impact millions globally. You will be part of a dynamic team committed to excellence in clinical trial management and regulatory compliance.

- MBBS or MD qualification - 3 to 14 years of pharmacovigilance experience - Medical review expertise in AR and RMP reports - Signal management knowledge - Expert English proficiency - Compliance and quality management skills - Clinical trial knowledge - Project planning experience - Healthcare industry understanding

- Full-time permanent employment - Professional development opportunities - Training and skill enhancement programs - Knowledge sharing and mentoring opportunities - Healthcare industry exposure - Compliance with global regulatory standards