Eli Lilly and Company Pharmacovigilance Manager life
sciences, Masters ( Science/Pharma), BDS
Perform case management activities which includes but not
limited to
Review of the safety data from various sources
Identifying adverse events, seriousness and listedness of the
events.
Performing complete and accurate entry of all safety data
with medDRA coding and a brief narrative of the safety information
Forwarding AE report for medical review as appropriate
Following up for safety information as relevant
Ensure compliance to internal and external timelines for
managing AE data entry and expedited reporting as appropriate
Develop and update standard operating procedures and training
tools/programs as necessary
Support and collaborate effectively with internal/external
customers such as medical reviewers, surveillance teams, call center contacts,
affiliate office, legal, clinical trial management, etc.
Provide training/mentoring/coaching to new employees
Responsibilities may vary depending on the needs and focus of
a particular team and additional responsibilities may be assigned based on the
team/unit/organizational need.
Qualification
Graduate Degree (or higher) in a healthcare related field or
life sciences, Masters ( Science/Pharma), BDS.
Good knowledge of disease states and drugs, pharmacovigilance
and global regulations
Competency in IT platforms including databases, MS office,
internet search, etc.
Effective communication (written and verbal)
Attention to detail, analytical and problem solving skills
Ability to perform multitasking with prioritization and
decision making
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