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Remote Pfizer Medical Writer Jobs in Florida (NOW HIRING)

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Remote Pfizer Medical Writer information

What is the difference between Remote Pfizer Medical Writer vs Remote Medical Science Liaison?

AspectRemote Pfizer Medical WriterRemote Medical Science Liaison
Required CredentialsMedical degree or life sciences background, writing certificationsMedical or scientific degree, often with clinical or research experience
Work EnvironmentCollaborates with medical teams, writes regulatory and scientific documentsEngages with healthcare professionals, provides scientific education
Employer & Industry UsagePharmaceutical companies, biotech firms, regulatory agenciesPharmaceutical companies, medical organizations, biotech firms

Remote Pfizer Medical Writers focus on creating scientific and regulatory documents within pharmaceutical companies, while Remote Medical Science Liaisons primarily engage with healthcare professionals to communicate scientific information. Both roles require strong scientific credentials but differ in daily tasks and interactions.

What are the most commonly searched types of Pfizer Medical Writer jobs in Florida? The most popular types of Pfizer Medical Writer jobs in Florida are:
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Infographic showing various Remote Pfizer Medical Writer job openings in Florida as of July 2026, with employment types broken down into 51% Part Time, and 49% Contract. Highlights an 100% Remote job distribution.

Medical Writer / Clinical Document Author

micro1 AI

Tampa, FL • Remote

$50 - $80/hr

Part-time

Posted 5 days ago

Job description

Role Title: Medical Writer / Clinical Document Author


Role Type: Contractor


Location: Remote


micro1 is engaging Medical Writers / Clinical Document Authors to participate in a customer’s project focused on developing advanced AI-assisted writing tools for clinical documentation. In this role, you'll apply your expertise to help train next-generation AI systems. Your work will shape how models learn, reason, and perform through high-quality, real-world input. No prior experience in AI is required — your domain knowledge is what matters.


Scope of Work

  1. Author and review realistic evaluation tasks based on Clinical Study Reports, DSURs, PSURs/PBRERs, and related clinical documents to inform AI tool development.
  2. Apply expert judgment to assess whether AI-generated content fulfills clinical template and structural requirements, including ICH E3 organization, section sequencing, cross-referencing, and appendix management.
  3. Evaluate scientific accuracy in narrative sections such as efficacy, safety summaries, discussion, and conclusions, distinguishing true scientific or interpretive errors from stylistic differences.
  4. Trace narrative claims to source records—tables, figures, listings, and protocols—to verify that all assertions are appropriately supported.
  5. Provide clear and structured written rationales for each assessment, enabling precise diagnosis and improvement of AI model behavior.
  6. Collaborate with project leads to refine evaluation frameworks and document best practices for clinical regulatory writing in the context of AI.


Preferred Qualifications

  1. Minimum 5 years of regulatory medical writing experience at a sponsor, CRO, or as an independent consultant.
  2. Direct experience independently authoring or leading the authoring of full Clinical Study Reports, beyond summaries or partial contributions.
  3. Fluency with ICH E3 and conventions for periodic safety documentation (ICH E2F, ICH E2C) and eCTD placement.
  4. Demonstrated ability to read and interpret TFLs and protocol documents, identifying where narrative diverges from source data.
  5. Exceptional written and verbal communication skills, especially in providing structured, actionable feedback on clinical content.
  6. Advanced degree in life sciences, pharmacy, or medicine (PhD, PharmD, MD, MSc), or equivalent depth of authoring experience.
  7. Experience across multiple clinical phases and therapeutic areas; oncology and haematology expertise is especially valued.


Join our customer's team and leverage your authoring expertise to help design the next generation of AI-assisted clinical documentation solutions. This high-bar role offers you the chance to shape how tomorrow's writing teams draft and review regulatory documents — through your expert input, judgment, and real-world experience.

Apply