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Medical Writer

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Job Title: Medical Writer

Location: Remote

Duration: 12 Months

Client: AbbVie

Experience: 5 yrs

Job Description:

  • 5 plus yrs. exp in industry with medical writing will be overqualified.
  • Solid written and verbal communication skills
  • Someone with industry exp will be considered as well.
  • This role is not for writing regulatory submissions.
  • Publications writing role.
  • Will be working on manuscript abstract posters and journals.
  • Fresh Phd grad will also work.
  • Therapeutic areas: migraine neuro Parkinson disease Alzheimers immunology within dermatology space
  • PhD preferred in science field or other advanced degree with scientific writing experience.
  • Scientific background needed
  • Summary

    The Senior Medical Writer is responsible for providing medical writing ensuring successful preparation of highquality documents and effective implementation of the writing process.

    Provides medical writing expertise for multiple compounds and/or projects within a therapeutic area. Interfaces with crossfunctional groups to ensure accurate and timely completion/delivery of information and review of writing projects

    Responsibilities:

  • Serves as medical writing lead on assigned projects. Works closely with infunction and crossfunctional team(s) on project strategies. Implements all activities related to the preparation of writing projects
  • Coordinates the review approval and other appropriate functions involved in the production of writing projects.
  • Arranges and conducts review meetings with the team.
  • Ensures required documentation is obtained.
  • Converts relevant data and information into a form that meets project requirements.
  • Explains data in a manner consistent with the target audience(s) requirements.
  • Effectively communicates deliverables needed writing process and timelines to team members.
  • Holds team members accountable to agreedupon project dates and with an appropriate quality level.
  • Negotiates with functional areas on project outcomes and deliverables to meet conflicting demands.
  • Identifies and proposes solutions to resolve issues and questions arising during the writing process including resolution or elevation as appropriate.
  • Understands assimilates and interprets sources of information with appropriate guidance/direction from development teams. Interprets and explains data generated from a variety of sources.
  • Verifies that results are consistent with protocols.
  • Challenges conclusions when necessary. Understands/complies with appropriate conventions proper grammar usage and correct format requirements as needed for each writing project following applicable divisional guidelines templates and SOPs.
  • Performs literature searches as needed for drafting document content. Interprets literature information and makes recommendations for application to writing projects.
  • Works with journal/congress throughout the writing process addresses questions/feedback as appropriate and works with a team to draft responses as necessary.
  • Knowledgeable of US and international regulations requirements and guidance associated with preparation of writing projects. Learns and applies knowledge of therapeutic areas and products to writing projects. Must continually train/be compliant with all current industry requirements as they relate to assigned projects including submission/approval standards.
  • Serves as a representative on project teams.
  • Acts as Subject Matter Expert regarding computerbased technologies utilized by the respective departments.
  • May mentor and provide guidance to more junior medical writers and/or external vendors/agencies. Implements tactical process improvements
  • Qualifications

    • Bachelor of Science required with relevant writing experience or Bachelors degree in English or communications with relevant science experience. Advanced degree preferred.
    • American Medical Writing Association (AMWA) certification or other is preferred with a specialty in Editing/Writing or Pharmaceutical.
    • 3 years relevant industry experience in medical writing in the healthcare industry or academia required or in a related area such as quality regulatory publications clinical research or product support/R&D.
    • 3 years experience in experimental design and clinical/preclinical data interpretation preferred.
    • Knowledgeable of US and international regulations requirements and guidance associated with preparation of assigned writing projects.
    • Knowledge and experience working with templates and relevant systems
    • Excellent written and oral communication skills. Experience in working with collaborative crossfunctional teams including project management experience.
    • Ability to assimilate and interpret scientific content and translate information for appropriate audiences.
    • Superior attention to detail. Ability to find and correct errors in spelling punctuation grammar consistency clarity and accuracy.
    • Expert in word processing flow diagrams and spreadsheets. Excellent working knowledge of software programs in the Windows environment

    نوع التوظيف

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