[Solo Quedan 15h] Product Surveillance Analyst...

Job Description

• In conjunction with the Clinical Safety and Risk Management (CSRM) team, works to expand and apply clinical, pharmacological, and epidemiologic knowledge and information technology skills to managing the safety surveillance for assigned products.
• Performs safety surveillance review of adverse experience reports as per SOP with the CSRM team in order to assist with the monitoring and description of the safety profile of assigned products and to identify and respond to safety issues.
• Prepares responses to safety inquiries from health care professionals, regulatory agencies, subsidiary staff and other internal customers in conjunction with the CSRM team assigned to the product.
• Develops working knowledge of pharmacovigilance and Risk Management Plans; begins to educate stakeholders outside or CSRM about risk management and role of CSRM.
• Core member of Risk Management Safety Team (RMST). Represents CSRM on cross functional teams and committees as appropriate. Assists the CSRM team with the development and evaluation of Risk Management Plans (RMP) and Risk Evaluation and Mitigation Strategies (REMS) for assigned products.
• Assists in the preparation of manuscripts for submission to peer reviewed journals and gives poster and oral presentations at medical conferences on the safety profile of assigned products. Assists with the guidance of these documents through the internal clearance and external submission process.
• Participates in the development, implementation and evaluation of standards, processes, metrics and other department initiatives.

Requirements

Requisition ID : R367022

Job Posting End Date : 10 / 11 / 2025

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