Pharmacovigilance Services Specialist

Role Overview Accenture is looking for a Pharmacovigilance Services Specialist to join its Life Sciences R&D vertical. This role sits within the Clinical, Pharmacovigilance and Regulatory sub-offering and supports the world's leading biopharma companies in delivering safer, more effective medicines to patients. The specialist will contribute to medical affairs solutions while working at the intersection of scientific expertise and patient-centered care. Key Responsibilities - Analyze and resolve moderately complex pharmacovigilance and medical affairs challenges, developing tailored business solutions as needed - Design and deliver services related to the medical affairs function, including thought leadership development, medical publications, education and information programs, medical grants, advisory boards, and advocacy initiatives - Monitor and analyze safety data from clinical trials, healthcare providers, and patients to detect, assess, and help prevent adverse effects linked to pharmaceutical products - Understand and align with the strategic direction set by senior management with respect to team and client goals - Manage small teams or work independently as an individual contributor on client engagements or internal Accenture projects - Collaborate with peers and management across client organizations and within Accenture to drive outcomes Required Qualifications - MBBS degree is mandatory - 0 to 4 years of experience in pharmacovigilance, medical affairs, or a related life sciences domain - Strong analytical mindset with the ability to solve moderately complex problems independently - Willingness and ability to work in rotational shifts - Team-oriented with adaptability and a capacity for quick learning Why Join Us Accenture's Life Sciences practice offers a dynamic environment where you can grow your expertise in pharmacovigilance while contributing to solutions that directly improve patient outcomes globally. You will work alongside some of the brightest minds in biopharma consulting, with structured guidance and clear paths for career progression.

- MBBS qualification - 0 to 4 years of experience in pharmacovigilance or medical affairs - Ability to analyze and solve moderately complex problems - Understanding of regulatory and patient safety requirements in the pharmaceutical industry - Willingness to work rotational shifts - Strong team collaboration and communication skills - Adaptable and quick to learn new methods and procedures

- Opportunity to work with leading global biopharma companies - Exposure to end-to-end life sciences operations including clinical trials, regulatory services, and patient solutions - Structured mentorship and guidance from senior management - Full-time permanent employment with a globally recognized organization