Pharmacovigilance Openings – Bangalore (0–11 Years)
Location: Bangalore, India (Work From Office)
Experience: 0–11 Years
Eligibility: B.Pharm / M.Pharm / Pharm.D graduates
Not Eligible: Candidates who have applied within the last 1 year
Company: Accenture
Apply By: Send CV to ravusala@gmail.com
About the Role
Accenture is hiring passionate and detail-oriented professionals for Pharmacovigilance (PV) roles in Bangalore. This is an excellent opportunity for candidates at all experience levels (freshers to experienced professionals) to gain exposure in drug safety, clinical trial monitoring, and adverse event reporting.
Key Responsibilities
Case Processing: Handle Individual Case Safety Reports (ICSRs), adverse event reporting, and database entry.
Medical & Literature Review: Assist in evaluation and documentation of safety data from clinical trials and post-marketing sources.
Compliance & Reporting: Ensure adherence to regulatory guidelines (FDA, EMA, ICH) and internal Standard Operating Procedures (SOPs).
Collaboration: Work with cross-functional teams, including clinical operations, medical affairs, and data management.
Audit & Quality Support: Participate in audits, inspections, and quality review processes.
Required Skills
Strong knowledge of pharmacovigilance principles and drug safety processes.
Proficiency in case management systems and safety databases.
Good analytical, problem-solving, and communication skills.
Attention to detail and ability to work in a fast-paced environment.
English fluency (spoken & written).
Benefits
Gain experience in a global consulting environment.
Exposure to end-to-end PV operations across therapeutic areas.
Opportunity to work with industry-leading professionals in healthcare and life sciences.
How to Apply
Send your updated CV to: ravusala@gmail.com
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