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Are you passionate about pharmaceutical research and pharmacovigilance? AstraZeneca invites applications for the Literature Review Advisor role in Bangalore, India. This full-time position offers a unique opportunity to contribute to drug development, regulatory submissions, and clinical practice through high-quality literature review and data analysis. Be part of a global team leveraging digital platforms, cutting-edge technology, and scientific expertise to transform lives.
Key Responsibilities
Literature Review & Data Analysis
- Conduct comprehensive literature searches using AstraZeneca databases.
- Ensure accuracy and reconciliation of pharmacovigilance data.
- Identify, collect, and analyze scientific publications, clinical studies, and regulatory reports.
- Stay updated with automation and technology trends in literature searches.
Collaboration & Cross-Functional Support
- Work with Marketing, R&D, Regulatory, Medical Affairs, and Clinical Operations teams.
- Develop scientifically sound literature materials, summaries, and reports.
- Collaborate with external institutions and academic partners on literature review tasks.
Regulatory & Compliance Adherence
- Contribute to Good Pharmacovigilance Practice (GVP) in line with safety-related processes.
- Support external service providers in meeting local regulatory PV requirements.
- Maintain knowledge of global and local procedural guidance, marketed product status, and safety obligations.
Qualifications & Skills
Essential Skills
- Strong knowledge of pharmacovigilance and GVP.
- Understanding of health authority regulations.
- Effective cross-functional collaboration, lateral thinking, and problem-solving.
- Vendor management experience.
- Excellent attention to detail and communication skills.
Desirable Skills
- Influencing and conflict resolution abilities.
- Medical knowledge in company Therapeutic Areas.
- Project management and audit experience.
- Successful participation in above-market projects.
Benefits
- Work in a dynamic, innovative, and digital-driven pharmaceutical environment.
- Opportunity to collaborate with global teams and subject matter experts.
- Flexible in-office policy with at least three days/week in Bangalore.
- Contribute to life-changing medicines impacting patient outcomes.
Application Instructions
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