Manager, Medical Information
New
S
SequelMedical devices
Listing location: Marlborough, MA / Manchester, NH; Workplace type: RemoteFull-TimeManager
Salary75,000 - 140,000 USD per year
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Job Details
- Experience
- 5+ years of relevant industry experience in medical safety, pharmacovigilance, clinical research, or medical affairs.
Requirements
- Advanced degree in medicine, pharmacy, nursing, or life sciences (MD, PharmD, PhD, NP, PA, or equivalent).
- 5+ years of relevant industry experience in medical safety, pharmacovigilance, clinical research, or medical affairs.
- Experience in the medical device and/or pharmaceutical industry, with exposure to post-market surveillance and safety reporting.
- Strong writing and editing skills for medical response letters, scientific summaries, and healthcare professional-facing content.
- Experience developing and maintaining standard response documents, FAQs, and medical information repositories.
- Familiarity with the Medical, Legal, and Regulatory review process and standards for promotional and scientific materials.
- Ability to interpret clinical and real-world data, including study endpoints, confidence intervals, and effect sizes.
- Ability to translate scientific evidence into clear, unbranded educational content for healthcare professional audiences.
- Ability to collaborate across Medical Affairs, Regulatory, Marketing, and Commercial teams.
- Ability to manage multiple projects, prioritize effectively, and deliver under tight timelines.
- Strong influencing, facilitation, and presentation abilities.
Responsibilities
- Respond to verbal and written medical inquiries from internal and external customers.
- Develop and revise standard medical response letters and maintain the medical information repository, FAQs, and reference materials.
- Work with Medical Affairs colleagues, including medical directors, scientists, and the Chief Medical Officer, to gather and verify information.
- Coordinate with marketing and public relations teams to align medical communications with company messaging.
- Proofread and edit medical content and implement quality control measures.
- Manage medical content preparation and submission to the Medical, Legal, and Regulatory and Scientific Material Review processes.
- Review promotional materials containing medical content for medical accuracy and track reviewer feedback and revisions.
- Create unbranded presentations and scientific summaries for Medical Education and healthcare professional audiences.
- Compile and synthesize healthcare professional insights to inform scientific and education priorities.
- Ensure communications and medical information resources comply with regulatory requirements and ethical standards.
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