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Medical Writer
Medical WriterHMP Global • Malvern, PA, US
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Medical Writer

Medical Writer

HMP Global • Malvern, PA, US
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  • [job_card.full_time]
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Job Description

HMP Global is an industry leader in providing CME activities for healthcare practitioners across a broad range of therapeutic areas. We are currently seeking a Medical Writer/Editor to join our growing team.


The Medical Writer/Grant Proposal Writer will play a vital role in our educational programming organization by writing and revising educational grant requests/proposals. You will collaborate with Business Development, Grants, and Outcomes colleagues to plan and assess educational activities.


Please be prepared to submit writing samples when requested.


Responsibilities:

  • Overall development, writing, and editing of grant proposals to assure submission on or before deadlines (learning objectives, agenda, educational design, educational gap analysis, clinical needs assessment)
  • Regularly revise developed proposals based on updates within the therapeutic area
  • Maintain a working knowledge of latest clinical data and FDA approvals within company’s therapeutic areas of interest
  • Review educational content prepared by faculty and develop outcomes questions based on final program content


Experience and Educational Requirements:

  • Bachelor’s degree in medical/scientific area (required); advanced degree (e.g., MS, PhD, MPH) or at least 2 years of experience as a medical writer (required)
  • Clinical writing experience (preferred, not required)
  • Verifiable and consistent work history (required)
  • Experience and demonstrated success with grant, proposal, abstract and manuscript writing
  • Ability to complete literature review and review/analyze scientific/medical research in order to apply knowledge to content development


Minimum Skills, Knowledge and Ability Requirements:

  • Deadline driven, capable of working in a fast-paced environment
  • Ability to search, interpret, and summarize published literature
  • Basic understanding of clinical trial design and drug approval process in the US and Europe
  • Proficiency with using Microsoft Office suite (e.g., Word, PowerPoint, Excel)
  • Ability to manage several projects simultaneously: excellent time management and organizational skills
  • Strong attention to detail; high level of accountability
  • Excellent communication skills: ability to communicate effectively both orally and in writing
  • Solid teamwork and interpersonal skills
  • Excellent command of the English written language including grammar, punctuation, etc.
  • Ability to work both independently and in a collaborative environment
  • Consistent and verifiable work history


Please follow HMP Global on LinkedIn for news and updates

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Medical Writer • Malvern, PA, US

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