Pharmacovigilance Services New Associate
Location: Bengaluru, India
Job Type: Full-Time
Job ID: AIOC-S01630316
Company: Accenture
Experience Required: 0–2 Years
Qualification: MSc or Master of Pharmacy (M.Pharm)
About Accenture
Accenture is a global professional services company with strong capabilities in digital transformation, cloud technologies, and cybersecurity. With a workforce of more than 784,000 professionals serving clients across 120+ countries, Accenture delivers services in Strategy and Consulting, Technology, Operations, and Accenture Song.
In the life sciences sector, Accenture supports pharmaceutical and biotechnology companies across the entire research and development lifecycle, including clinical research support, regulatory services, pharmacovigilance, and patient services. The company focuses on combining scientific expertise with advanced technologies to improve patient outcomes and accelerate innovation in healthcare.
Job Overview
Accenture is hiring a Pharmacovigilance Services New Associate for its Life Sciences R&D division in Bengaluru. This entry-level role is suitable for candidates with a life sciences background who are interested in building a career in pharmacovigilance, drug safety monitoring, and regulatory compliance.
The selected candidate will support pharmacovigilance operations by assisting in adverse event case processing, safety data management, and regulatory reporting while ensuring compliance with global pharmacovigilance guidelines.
Key Responsibilities
Perform case identification and accurate data entry for Individual Case Safety Reports (ICSRs) in pharmacovigilance safety databases.
Conduct MedDRA coding for adverse events and medical information.
Support case processing, quality review, and submission of safety reports according to client guidelines and global regulatory requirements.
Manage case follow-ups and maintain complete documentation of safety information.
Ensure adherence to pharmacovigilance regulations, SOPs, and internal quality standards.
Collaborate with internal teams to ensure timely and accurate safety reporting.
Maintain high standards of data accuracy and compliance in pharmacovigilance processes.
Required Skills and Competencies
Basic understanding of Pharmacovigilance and Drug Safety Surveillance.
Knowledge of adverse event reporting and ICSR processing.
Familiarity with MedDRA terminology is an advantage.
Strong attention to detail and analytical skills.
Good written and verbal communication abilities.
Ability to work in a structured process-driven environment.
Roles and Responsibilities
Handle routine pharmacovigilance tasks using standard procedures and guidelines.
Work closely with team members and report to the direct supervisor for task guidance.
Perform assigned activities with detailed instructions and defined processes.
Contribute as an individual team member with a focused scope of work.
Ensure all work is completed according to quality standards and compliance requirements.
Be flexible to work in rotational shifts based on business requirements.
Why Join This Role
This role provides an excellent opportunity for early-career professionals to gain practical exposure to pharmacovigilance operations, drug safety surveillance, and regulatory compliance in a global life sciences environment. Candidates will develop skills in safety database management, adverse event reporting, and global pharmacovigilance standards while contributing to patient safety worldwide.
Job Location
Bengaluru, India.
Uttar Pradesh :
Agra | Gajraula | Gautam buddha Nagar | Ghaziabad | Gorakhpur | Greater Noida | Jhansi | kanpur | Lucknow | Mathura | Noida | Park City | Prayagraj | Satyamev | Varanasi |Gujarat :
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Auckland |New Zealand :
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