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Job description
AbbVie is seeking a Principal Medical Writer to lead and write clinical and regulatory documents for drug and/or device development to support company objectives. You will coordinate cross-functional review, ensure timelines, maintain inspection-ready documentation, and apply US and international regulatory guidance.
The role requires 5+ years in bio-pharma with strong writing skills, attention to detail, and ability to manage multiple projects across teams.
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Who can apply
Review the original listing for work authorization, qualifications and employer requirements.