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Remote Science Content Developer Jobs in Manchester, NH

micro1 AI

Medical Writing Manager

Manchester, NH · Remote

$50 - $80/hr

Remote micro1 is engaging Medical Writers / Clinical Document Authors to participate in a customer ... content. * Advanced degree in life sciences, pharmacy, or medicine (PhD, PharmD, MD, MSc), or ...

Varsity Tutors

FE - Civil Engineering Tutor

Lawrence, MA · Remote

$18 - $40/hr

Deep knowledge of FE Civil examination content covering mathematics, probability and statistics ... science to create personalized learning experiences. Through 1-on-1 Online Tutoring, students ...

GEI Consultants

Senior Structural Engineer

Bedford, NH · On-site +1

$100K - $160K/yr

... two days remote). Dams in our clients' portfolios are in some of the most spectacularly scenic ... With several offices across North America, we offer a range of engineering, science, and technical ...

Varsity Tutors

ChatGPT Tutor

Lawrence, MA · Remote

$18 - $40/hr

... engineering, conversational AI interaction, content generation, code assistance, data analysis ... science to create personalized learning experiences. Through 1-on-1 Online Tutoring, students ...

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How much do remote science content developer jobs pay per year?

As of Aug 22, 2026, the average yearly pay for remote science content developer in Manchester, NH is $116,111.00, according to ZipRecruiter salary data. Most workers in this role earn between $122,500.00 and $127,400.00 per year, depending on experience, location, and employer.

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Remote Science Content Developer jobs near you
Infographic showing various Remote Science Content Developer job openings in Manchester, NH as of August 2026, with employment types broken down into 54% Full Time, 24% Part Time, and 22% Contract. Highlights an 100% Remote job distribution, with an average salary of $116,111 per year, or $55.8 per hour.

Medical Writing Manager

micro1 AI

Manchester, NH • Remote

$50 - $80/hr

Part-time

Posted 18 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