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Job Requirements of Senior Medical Information Specialist:
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Employment Type:
Contractor
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Location:
Nutley, NJ (Onsite)
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Senior Medical Information Specialist
Sr. Medical Information Specialist
Nutley, NJ/Hybrid- (Tues, Wed and Thurs)
Duration: 12 Months+
Shift: 1st Shift
Pay range $60-$62.50/hr on w2
HM Must have Skills:
Advance Degree: PharmD/Phd/MD
Job Profile: medical information/Medical communications/ scientific communication/Medical Affairs
Hands-On experience: Medical writing/ Writing/Scientific writing/literature evaluation and summarization
Therapeutic: Oncology experience Must have.
Years of exp: 1-3 years of experience in pharmaceutical industry
Job description:
The position will be hybrid requiring three days per week in the office (Tues, Wed and Thurs) at our Nutley location.
The Senior Medical Information Specialist is responsible for meeting the medical information needs of external customers and internal business partners. He/she will respond to medical inquiries, contribute to the development of high-quality Medical Information deliverables, and will be responsible for scientific accuracy review of assigned promotional and scientific exchange materials. This includes but is not limited to:
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 ***s 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 *** 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
Knowledge/Skills Required:
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