Medical Information Specialist, Eisai Inc – NJ
Eisai Inc is seeking a Medical Information Specialist. The Medical Information Specialist/Manager is responsible for meeting the medical information needs of external customers and internal business partners as it relates to the company’s products. He/she will contribute to the development of high quality medical information deliverables within the team and will be a visible member of the department by collaborating cross-functionally to meet Medical Affairs objectives. Primary job functions include:• Utilize clinical and scientific expertise to respond to medical information inquiries from health care professionals, patient/consumers, field staff , internal business partners and other customers
• 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
• Contribute to the development and revision of standard medical responses, AMCP dossiers, Q
& A documents and other medical information resources
• Ensure medical accuracy of Eisai’s advertising, promotional and scientific materials as part of Copy
Review Committee and Product Medical Review Committee (in collaboration with Medical Information Managers and Medical Directors for Medical Information Specialist)
• Assist with and contribute to other Scientific Communications and Medical Affairs activities
Depending on level of experience, may have responsibility for:
• Lead medical information activities for assigned products
• Serve as medical and therapeutic area expert for assigned products; conduct training for
Medical Affairs colleagues and cross-functionally
• Develop strategic medical plans for assigned products in collaboration with Medical Director and other Medical Affairs colleagues
• Serve as project lead for development of AMCP dossiers for assigned products
Partner with Medical Director for other Medical Affairs activities
Qualifications:
Biomedical training and education (RPh, – PharmD preferred)
• Superior literature database search skills
• Excellent written and verbal communication skills with experience in medical writing
• Superior customer service skills
• Knowledge of US regulatory standards related to pharmaceutical manufacturers’ communications and dissemination of medical information, clinical trials processes & drug approval processes
• Minimum of 1 year of experience in pharmaceutical industry-based medical information or related discipline for Specialist
• Familiarity with Microsoft Office software and customer management software
To apply: https://sjobs.brassring.com/1033/ASP/TG/cim_jobdetail.asp?jobId=416607&partnerid=25064&siteid=5015&codes=Indeed
