Senior Medical Information Specialist Job at SGS Consulting, New Jersey

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  • SGS Consulting
  • New Jersey

Job Description

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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