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Director Remote Medical Writing Jobs in Oregon (NOW HIRING)

Remote micro1 is engaging Medical Writers / Clinical Document Authors to participate in a customer ... Direct experience independently authoring or leading the authoring of full Clinical Study Reports ...

Remote micro1 is engaging Medical Writers / Clinical Document Authors to participate in a customer ... Direct experience independently authoring or leading the authoring of full Clinical Study Reports ...

Remote micro1 is engaging Medical Writers / Clinical Document Authors to participate in a customer ... Direct experience independently authoring or leading the authoring of full Clinical Study Reports ...

The Associate Scientific Director will oversee the development of technically accurate and high ... Minimum of 4-5+ years' medical writing experience in an agency or pharmaceutical company setting

Remote micro1 is engaging Medical Writers / Clinical Document Authors to participate in a customer ... Direct experience independently authoring or leading the authoring of full Clinical Study Reports ...

Remote micro1 is engaging Medical Writers / Clinical Document Authors to participate in a customer ... Direct experience independently authoring or leading the authoring of full Clinical Study Reports ...

Medical Director

$225K - $275K/yr

Excellent verbal and written communication skills. * Proficient with Microsoft Office Suite (Word ... Remote #director Employment Type: OTHER

Exceptional presentation, interpersonal, verbal and written communication skills. * Superior ... This remote role can be located anywhere in the continental US. * Remaining in a stationary ...

Remote with ~40% domestic and international travel Shape the future of cancer care as a Medical ... Strong written and verbal communication skills, including scientific presentation and education.

Effective technical writing and communication * Proficient and experienced in utilization of cloud ... NV5 offers competitive compensation and benefits package including medical, dental, life insurance ...

Showing results 21-40

Director Remote Medical Writing information

What is the difference between Director Remote Medical Writing vs Medical Writing Manager?

AspectDirector Remote Medical WritingMedical Writing Manager
CredentialsTypically requires advanced degrees (MD, PhD, PharmD) and extensive medical writing experienceRequires similar credentials but may have slightly less experience or seniority
Work EnvironmentLeads remote medical writing teams, collaborates with cross-functional teams, and oversees project strategyManages medical writing staff, reviews documents, and ensures quality and compliance
Industry UsageCommonly used in pharmaceutical, biotech, and healthcare industries for strategic oversightUsed across similar industries for team management and project execution

The main difference is that the Director Remote Medical Writing typically holds a higher strategic leadership role with broader responsibilities, while the Medical Writing Manager focuses more on team management and document quality. Both roles require strong medical writing credentials and industry experience, but the director position involves more oversight and strategic planning.

What are the most commonly searched types of Remote Medical Writing jobs in Oregon? The most popular types of Remote Medical Writing jobs in Oregon are:
What are popular job titles related to Director Remote Medical Writing jobs in Oregon? For Director Remote Medical Writing jobs in Oregon, the most frequently searched job titles are:
What job categories do people searching Director Remote Medical Writing jobs in Oregon look for? The top searched job categories for Director Remote Medical Writing jobs in Oregon are:
What cities in Oregon are hiring for Director Remote Medical Writing jobs? Cities in Oregon with the most Director Remote Medical Writing job openings:

Medical Billing Specialist

micro1 AI

Bend, OR • 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.