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Job Posting: Pharmacovigilance Services Associate


Job Number: AIOC-S01509165


About Accenture

About the Company: Accenture is a global professional services company with leading capabilities in digital, cloud, and security. Combining unmatched experience and specialized skills across more than 40 industries, Accenture offers Strategy and Consulting, Technology and Operations services, and Accenture Song – all powered by the world’s largest network of Advanced Technology and Intelligent Operations centers. With 699,000 employees serving clients in over 120 countries, Accenture embraces the power of change to create value and shared success for clients, people, shareholders, partners, and communities. For more information, visit accenture.com.

Skills Required: Pharmacovigilance Operations – Pharmacovigilance & Drug Safety Surveillance

Designation: Pharmacovigilance Services Associate

Qualifications: Bachelor of Pharmacy/Master of Pharmacy/Master Of Physiotherapy

Years of Experience: 1 to 3 years

What would you do? The Pharmacovigilance Case Processing Associate is responsible for the timely and accurate processing of ICSR cases. This includes data entry, narrative writing, case follow-up, and submission per global regulatory guidelines.

What are we looking for? Bachelor’s Degree in Life Science or Healthcare related field – 0-2 years of pharmacovigilance experience preferred – Excellent written communication and interpersonal skills

– Proficient in medical terminology – Meticulous attention to detail and accuracy – Ability to handle large volumes and tight timelines – Strong knowledge of pharmacovigilance guidelines and regulations

Roles and Responsibilities:

  • Enter adverse event case data into the safety database accurately and completely
  • Retrieve additional case information by contacting reporters/physicians as needed
  • Write clear, coherent, and scientifically sound adverse event case narratives
  • Assess seriousness, severity, causality and expectedness for individual cases
  • Determine reportability of cases and submit expedited and periodic reports to regulators
  • Classification of medical conditions and assignment of MedDRA codes for cases
  • Follow up with reporters/physicians for missing case information as applicable
  • Comply with all global regulatory reporting requirements and company procedures
  • Maintain up-to-date knowledge of changing safety regulations and guidelines

To apply for this position, visit the original notification here.

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