Pharmacovigilance Services New Associate (Drug Safety Associate Entry Level)

Pharmacovigilance Services New Associate (Drug Safety Associate Entry Level) Location: Bengaluru, India Company: Accenture Job ID: AIOC-S01628146 Job Type: Full-Time Experience Required: 02 Years (Freshers Eligible) About the Company Accenture is a leading global professional services organization specializing in digital, cloud, and security solutions. With operations in over 120 countries and a workforce of more than 700,000 professionals, Accenture delivers cutting-edge services across Strategy, Consulting, Technology, and Operations. Within Life Sciences, the organization plays a pivotal role in enabling pharmaceutical and biotechnology companies to accelerate innovation, ensure patient safety, and meet global regulatory standards. Job Overview This entry-level Pharmacovigilance role is part of Accentures Life Sciences R&D division, focusing on drug safety and risk management. The position is ideal for freshers and early-career professionals looking to build a strong foundation in Pharmacovigilance Operations, including Individual Case Safety Report (ICSR) processing and safety data management. Key Responsibilities Perform case identification, data entry, and processing of Individual Case Safety Reports (ICSRs) Conduct MedDRA coding and ensure accurate safety database entry Manage case workflows including follow-ups, submissions, and lifecycle tracking Monitor adverse drug reactions (ADRs) and support signal detection activities Ensure compliance with global pharmacovigilance regulations and client-specific guidelines Collaborate with internal teams for quality review and case closure Maintain data accuracy, completeness, and regulatory timelines in safety reporting Support routine pharmacovigilance operations under supervision Required Qualifications MSc (Life Sciences) / Bachelor of Pharmacy / Master of Pharmacy Strong understanding or academic exposure to Pharmacovigilance and Drug Safety Basic knowledge of MedDRA coding and ICSR lifecycle preferred Good analytical skills and attention to detail Effective communication and teamwork abilities Desired Skills and Competencies Understanding of Pharmacovigilance Operations and regulatory frameworks Familiarity with clinical research and drug safety processes Ability to work in a structured, process-driven environment Willingness to work in rotational shifts as per business requirements Work Environment and Role Scope Entry-level individual contributor role with defined responsibilities Tasks are guided by standard operating procedures and supervision Opportunity to gain hands-on experience in global pharmacovigilance projects Exposure to real-world drug safety case processing and regulatory workflows Why This Role is Important for Your Career This position serves as a gateway into the Pharmacovigilance and Drug Safety domain. It provides foundational experience in ICSR processing, regulatory compliance, and safety data handling, making it an ideal starting point for careers such as Drug Safety Associate, Medical Reviewer, or Pharmacovigilance Specialist. Equal Employment Opportunity Statement Accenture is committed to creating an inclusive workplace. All employment decisions are based on merit, qualifications, and business needs, without discrimination based on race, gender, age, disability, religion, sexual orientation, or any other protected status. How to Apply Candidates can apply through official company channels. For more verified Pharmacovigilance jobs for freshers and experienced professionals, visit ThePharmaDaily.com and explore global opportunities in Drug Safety, Clinical Research, and Regulatory Affairs. .