How you’ll spend your day
Participate in activities of literature review. Design and implement comprehensive literature search strategies on specific products. Knowledge of database: Embase, Medline, Pubmed, Ovid, etc.
Assess the impact of regulatory changes on the current process.
Contribute to simplification of processes.
Knowledge and expertise in Teva portfolio.
Support pharmacovigilance teams like case processing, trainings teams, quality assurance, audits and inspections etc.
Act as a consultant or SPOC for various case related activities and maintain knowledge repository of the process updates/ regulatory changes changes on real time.
Effective communications to be maintained with internal (related departments and units) & external (partners, authorities, vendors) stake holders in order to run the process as transparent as possible.
Ensure that quality data is analyzed for any trending and to prepare team for process stabilization.
Ensure regulatory compliance by following internal reporting key performance indicators for the unit are met.
Your experience and qualifications
Any life sciences/pharmaceutical/healthcare professional graduate (B. Pharmacy, M. Pharmacy, Pharm D, BDS).
Minimum of 4-6 years of experience in pharmacovigilance including literature review process in ICSR
Experience in patient safety/pharmacovigilance: solid knowledge in pharmacovigilance concepts, regulations, and procedures.
Advanced knowledge of Microsoft Office platforms.
Flexible to adapt to shifting team priorities.
