How much does a Drug Safety Medical Information Specialist make in the United States?

Supports drug safety assessment and medical information activities by evaluating adverse event reports, responding to medical inquiries, and ensuring compliance with pharmacovigilance regulations and company standards. Reviews, documents, and processes adverse event and product quality complaint reports to identify new, unknown, or changing risks associated with a drug or medicine. Evaluates drug safety data for completeness, accuracy, and potential signal detection activities in accordance with established procedures and regulatory timelines. Responds to medical information inquiries by providing accurate and scientifically supported product information to internal and external stakeholders. Maintains safety databases and prepares case narratives, summaries, and supporting documentation for regulatory submissions and internal review. Collaborates with cross-functional teams, including clinical, regulatory, quality, and medical affairs, to support product safety monitoring and risk management initiatives. Requires a bachelor's degree. Typically reports to a manager. Work is generally independent and collaborative in nature. Contributes to moderately complex aspects of a project. Typically requires 4-7 years of related experience. View Drug Safety Assessment Specialist III Salary

Supports drug safety assessment and medical information activities by evaluating adverse event reports, responding to medical inquiries, and ensuring compliance with pharmacovigilance regulations and company standards. Reviews, documents, and processes adverse event and product quality complaint reports to identify new, unknown, or changing risks associated with a drug or medicine. Evaluates drug safety data for completeness, accuracy, and potential signal detection activities in accordance with established procedures and regulatory timelines. Responds to medical information inquiries by providing accurate and scientifically supported product information to internal and external stakeholders. Maintains safety databases and prepares case narratives, summaries, and supporting documentation for regulatory submissions and internal review. Collaborates with cross-functional teams, including clinical, regulatory, quality, and medical affairs, to support product safety monitoring and risk management initiatives. Requires a bachelor's degree. Typically reports to a manager. Work is highly independent. May assume a team lead role for the work group. A specialist on complex technical and business matters. Typically requires 7+ years of related experience. View Drug Safety Assessment Specialist IV Salary

Supports drug safety assessment and medical information activities by evaluating adverse event reports, responding to medical inquiries, and ensuring compliance with pharmacovigilance regulations and company standards. Reviews, documents, and processes adverse event and product quality complaint reports to identify new, unknown, or changing risks associated with a drug or medicine. Evaluates drug safety data for completeness, accuracy, and potential signal detection activities in accordance with established procedures and regulatory timelines. Responds to medical information inquiries by providing accurate and scientifically supported product information to internal and external stakeholders. Maintains safety databases and prepares case narratives, summaries, and supporting documentation for regulatory submissions and internal review. Collaborates with cross-functional teams, including clinical, regulatory, quality, and medical affairs, to support product safety monitoring and risk management initiatives. Requires a bachelor's degree. Typically reports to a manager. Works autonomously. Goals are generally communicated in "solution" or project goal terms. May provide a leadership role for the work group through knowledge in the area of specialization. Works on advanced, complex technical projects or business issues requiring state of the art technical or industry knowledge. Typically requires 10+ years of related experience. View Drug Safety Assessment Specialist V Salary

Manages drug safety assessment programs and pharmacovigilance operations to ensure effective monitoring, evaluation, and reporting of product safety information across the organization. Directs adverse event processing, case review, aggregate reporting, and safety surveillance activities in compliance with global regulatory requirements and company policies. Develops and implements pharmacovigilance procedures, quality controls, and workflow improvements to enhance operational performance and regulatory readiness. Evaluates safety trends, signals, and risk data to support benefit-risk assessments and product safety strategies. Collaborates with clinical development, regulatory affairs, medical affairs, and quality teams to support product lifecycle safety management and regulatory submissions. Leads staff development, resource planning, vendor oversight, and audit preparation activities within the drug safety function. Requires a bachelor's degree. Typically reports to a director. Typically manages through subordinate managers and professionals in larger groups of moderate complexity. Provides input to strategic decisions that affect the functional area of responsibility. May give input into developing the budget. Typically requires 3+ years of managerial experience. Capable of resolving escalated issues arising from operations and requiring coordination with other departments. View Drug Safety Assessment Manager, Sr. Salary

Coordinates and administers clinical trials and research activities for medical product development. Recruits investigators, negotiates study details, and oversees human trials. Coordinates regulatory report submissions, monitors compliance, and concludes studies. May require an advanced degree. Typically reports to a manager. Work is generally independent and collaborative in nature. Contributes to moderately complex aspects of a project. Typically requires 4-7 years of related experience. View Medical Affairs Specialist III Salary