Accenture
Pharmacovigilance Services Specialist
- Eligibility
- Not stated
- Batch
- Not stated
- Experience
- 2–5 years
- Salary
- Not stated
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About this role
About the role: - Medical review of individual case safety reports, including assessment of adverse events, MedDRA coding, seriousness determination, and causality evaluation - Review of source documents for medical accuracy and identification of missing information - Support to clinical pharmacovigilance teams with medical expertise - Management of affiliate mailbox reconciliation and follow-up attempts for serious and non-serious cases - Ensure compliance with global pharmacovigilance regulations, standard operating procedures, audit requirements, and quality standards - May require rotational shift work What you'll do: - Analyze and solve moderately complex pharmacovigilance problems - Develop new solutions by adapting existing methods and procedures as needed - Work with direct supervisor and interact with peers and client management - Manage small teams or work efforts as assigned - Contribute to business solutions for pharmaceutical medical affairs including medical publications, education, medical grants, and advisory boards What they're looking for: - MBBS degree - 2 to 5 years of experience in pharmacovigilance - Experience with ICSR review, MedDRA coding, and WHO Drug - Knowledge of global safety reporting requirements - Medical Affairs expertise at P4 level Good to know: - Full-time role based in Chennai - Accenture is a global professional services company serving clients in more than 120 countries