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Accenture

Pharmacovigilance Services New Associate

1w

Accenture

Bengaluru, IN · Full-time · INR 400,000 – INR 700,000

About this role

You will be aligned with Accenture's Life Sciences R&D vertical. Services span research laboratories, clinical trials support, regulatory services, pharmacovigilance, and patient solutions. This role helps leading biopharma companies improve patient outcomes by connecting scientific expertise with patient insights.

Pharmacovigilance Services involve detection, assessment, and prevention of adverse effects related to pharmaceutical products. Create and manage case identification, data entry, MedDRA coding, case processing, submission, and follow-ups for ICSRs in the safety database. Follow client guidelines and global regulatory requirements to ensure medication safety.

In this role, solve routine problems largely through precedent and referral to general guidelines. Primary interaction is within your own team and direct supervisor. Receive detailed instructions on all tasks as an individual contributor with a narrow scope of work.

Accenture is a global professional services company with capabilities in digital, cloud, and security across more than 40 industries. Our 784,000 people serve clients in over 120 countries through the world's largest network of Advanced Technology centers. Embrace the power of change to create value for clients, people, and communities.

Requirements

  • Skill in Pharmacovigilance Services - Pharmacovigilance & Drug Safety Surveillance
  • BSc or Bachelor of Pharmacy
  • Knowledge of detecting, assessing, and preventing adverse effects of pharmaceutical products
  • Familiarity with monitoring data from clinical trials, healthcare providers, and patients
  • Ability to ensure compliance with regulatory requirements for medication safety
  • Experience handling ICSRs in safety databases (0 to 1 years)

Responsibilities

  • Create and manage case identification for ICSRs in the safety database
  • Perform data entry as per client guidelines and global regulatory requirements
  • Conduct MedDRA coding for pharmacovigilance cases
  • Process cases including assessment and analysis
  • Handle submission and follow-ups for ICSRs
  • Solve routine problems through precedent and general guidelines
  • Work under detailed instructions with close supervision
  • Participate in rotational shifts as required

Benefits

  • Work with world's leading biopharma companies
  • Part of global network serving clients in more than 120 countries
  • Powered by world's largest Advanced Technology and Intelligent Operations centers