Pharmacovigilance Services Associate
Job ID: AIOC-S01625968
Location: Bengaluru, India
Job Type: Full-Time
Company: Accenture
Experience Required
0–2 years (1–3 years of relevant experience in pharmacovigilance or drug safety preferred)
Educational Qualification
Bachelor of Pharmacy (B.Pharm) or Master of Pharmacy (M.Pharm).
Role Overview
Accenture is seeking a Pharmacovigilance Services Associate to support its Life Sciences Research and Development (R&D) division. The role focuses on pharmacovigilance operations, drug safety surveillance, and regulatory compliance activities to ensure the safe use of pharmaceutical products. The selected candidate will contribute to monitoring adverse drug reactions, managing safety data, and supporting global pharmacovigilance processes for leading biopharmaceutical organizations.
This position is ideal for pharmacy graduates and early career professionals seeking experience in drug safety, clinical research operations, and global regulatory compliance within a multinational professional services environment.
About Accenture
Accenture is a global professional services company with leading capabilities in digital, cloud, and security. With expertise across more than 40 industries, Accenture provides services in Strategy and Consulting, Technology, and Operations through the world’s largest network of Advanced Technology and Intelligent Operations centers. With a workforce of over 784,000 professionals serving clients in more than 120 countries, Accenture drives innovation and transformation through technology and human ingenuity.
Key Responsibilities
Perform case identification, data entry, and processing of Individual Case Safety Reports (ICSRs) in safety databases.
Conduct medical coding using MedDRA terminology in accordance with global regulatory standards.
Manage case processing, submission, and follow-up activities as per client guidelines and regulatory requirements.
Monitor and assess adverse drug reactions and drug safety data.
Ensure accuracy, completeness, and compliance of pharmacovigilance documentation.
Support safety data collection from clinical trials, healthcare providers, and patients.
Maintain high standards of data quality, regulatory compliance, and patient safety.
Collaborate with internal teams to ensure timely delivery of pharmacovigilance services.
Perform routine tasks based on established guidelines and standard operating procedures.
Work in rotational shifts as required by project needs.
Required Skills and Competencies
Knowledge of pharmacovigilance operations and drug safety surveillance processes.
Understanding of adverse event reporting and regulatory compliance standards.
Familiarity with MedDRA coding and safety database management.
Strong analytical and problem-solving skills.
Attention to detail and accuracy in data handling.
Ability to work effectively within a team environment.
Adaptability and willingness to learn in a dynamic work environment.
Work Environment and Expectations
Structured work environment with defined responsibilities and supervised learning.
Opportunity to work with global life sciences and pharmaceutical clients.
Exposure to regulatory services, clinical research operations, and pharmacovigilance processes.
Continuous professional development and career growth opportunities.
Equal Employment Opportunity
Accenture is committed to providing equal employment opportunities to all applicants without regard to race, religion, gender, disability status, sexual orientation, gender identity, or any other protected category in accordance with applicable laws.
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