Senior Medical Information Specialist
Job Responsibilities:
- Respond to medical information inquiries from health care professionals, patient/consumers, field staff, internal business partners, and other customers utilizing standard medical response documents or by creating ad hoc responses as appropriate
- Ensure medical accuracy of advertising, promotional and scientific materials as part of Copy Review Committee and Medical Review Committee, in collaboration with Medical Information Managers and Medical Directors; and ensure the scientific information is consistent with product labeling where appropriate Monitor scientific literature for potential adverse event reports, report findings to Product Safety within established timeframes
- Research and conduct detailed analyses of the scientific literature for Eisai marketed products, investigational compounds, competitor products/compounds, and related disease states. Contribute to communication, reporting, and storage of findings
- Develop, review, and/or update standard medical responses, AMCP dossiers, FAQ documents, and other medical information resources
- Provide scientific support for assigned stakeholders on ad hoc projects and/or initiatives
- Respond to medical information inquiries from health care professionals, patient/consumers, field staff, internal business partners, and other customers utilizing standard medical response documents or by creating ad hoc responses as appropriate
- Ensure medical accuracy of advertising, promotional and scientific materials as part of Copy Review Committee and Medical Review Committee, in collaboration with Medical Information Managers and Medical Directors; and ensure the scientific information is consistent with product labeling where appropriate Monitor scientific literature for potential adverse event reports, report findings to Product Safety within established timeframes
- Research and conduct detailed analyses of the scientific literature for Eisai marketed products, investigational compounds, competitor products/compounds, and related disease states. Contribute to communication, reporting, and storage of findings
- Develop, review, and/or update standard medical responses, AMCP dossiers, FAQ documents, and other medical information resources
- Provide scientific support for assigned stakeholders on ad hoc projects and/or initiatives
Skills:
- Advanced bioscience degree required (PharmD preferred)
- Demonstrated scientific knowledge and expertise, Oncology experience preferred
- Prior knowledge and understanding of US regulatory standards related to pharmaceutical manufacturers’ communications and dissemination of medical information
- Excellent verbal and written skills, with demonstrated experience in medical writing and development of scientific communication materials
- Superior literature database search skills, as well as expert literature evaluation and summarization skills
- Minimum of 1-3 years of experience in pharmaceutical industry-based medical information or related discipline
- Advanced bioscience degree required (PharmD preferred)
- Demonstrated scientific knowledge and expertise, Oncology experience preferred
- Prior knowledge and understanding of US regulatory standards related to pharmaceutical manufacturers’ communications and dissemination of medical information
- Excellent verbal and written skills, with demonstrated experience in medical writing and development of scientific communication materials
- Superior literature database search skills, as well as expert literature evaluation and summarization skills
- Minimum of 1-3 years of experience in pharmaceutical industry-based medical information or related discipline
Education/Experience:
- Advanced bioscience degree required (PharmD preferred)
- Advanced bioscience degree required (PharmD preferred)
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