Literature Surveillance and Reconciliation Analyst
Experience: 3+ Years | Location: Bangalore, Karnataka, India | Employment Type: Full-Time
Company Overview:
Join a global leader in healthcare, life sciences, and electronics, where science and technology intersect to improve lives. Our R&D Excellence Center in Bangalore fosters innovation, inclusion, and collaboration, offering you the opportunity to contribute to patient safety, pharmacovigilance, and scientific excellence on an international scale.
Role Overview:
As a Literature Surveillance and Reconciliation Analyst, you will be a vital part of the Global Patient Safety ICSR Management team. Your responsibilities include supporting literature surveillance processes, performing ICSR reconciliation, and maintaining high-quality safety information standards.
Key Responsibilities:
Support the business process owner in literature surveillance operations and process improvements.
Maintain and manage user access and training documentation for literature surveillance and reconciliation databases.
Perform operational activities, including reconciliation, quality checks (QC) of non-ICSR literature, and article uploads.
Conduct ICSR reconciliation, quality monitoring, and spot checks of safety information in collaboration with relevant functions.
Manage team mailboxes, ensuring timely action on all incoming communications.
Required Qualifications and Experience:
Medical or scientific degree (MBBS, B.Pharm, M.Pharm, or equivalent).
Minimum of 3 years of experience in a pharmacovigilance environment, with exposure to literature safety surveillance and ICSR reconciliation processes.
Sound understanding of global pharmacovigilance regulations for drugs in development and post-authorization.
Experience in ICSR case processing, preferably within the ArisG Safety Database.
Strong communication skills and the ability to collaborate in international and cross-cultural matrix teams.
Key Skills:
Attention to detail and strong analytical skills.
Ability to manage multiple tasks in a fast-paced, global environment.
Proactive problem-solving and process improvement mindset.
Why Join Us:
Work in a diverse, inclusive environment that celebrates innovation, collaboration, and excellence.
Gain global exposure in pharmacovigilance, literature surveillance, and patient safety processes.
Access professional growth opportunities, training programs, and a supportive work culture that empowers you to make an impact.
Apply Now: Take the next step in your pharmacovigilance career and join a global team dedicated to advancing patient safety and scientific progress.
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