Ensure compliance with applicable regulations and standard operating procedures in pharmacovigilance processes.
Specialize in drug safety management, clinical trials, and medical supervision.
Conduct, monitor, and report regular pharmacovigilance developments, overseeing processes related to drug effectiveness and adverse effects avoidance.
Aim to reduce risks associated with drug administration and prescribing, improving safety and treatment outcomes in patient care.
Perform important case report follow-up, process adverse event programs, and serve as a link between the company, healthcare experts, and patients to deliver valid information on product safety.
Conduct and supervise regular pharmacovigilance processes, attend product safety meetings, and enhance product safety functionality.
Monitor all products and conduct post-market evaluations to ensure drug safety, assess adverse event writings, update safety reports, and convey drug-related case reports to appropriate authorities.
Play a crucial role in research, development, and testing of new medications in the pharmaceutical industry.
Handle global pharmacovigilance activities, support data safety and case tracking, perform document archiving, assist in administering pharmacovigilance meetings, and support quality review of documents.
Draft pharmacovigilance agendas and meeting minutes, accurately archive documents, review safety case data for completeness and accuracy, monitor periodic safety reports, and assist with tracking, submitting, and distributing periodic reports.
Support liaisons with partners and cross-functional team members to ensure compliance, handle ad-hoc deliverables or pharmacovigilance projects, and assist with regulatory inspections.

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