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Remote Case Study Writer Jobs in Mississippi (NOW HIRING)

Medical Writer / Clinical Document Author Role Type: Contractor Location: Remote micro1 is engaging ... Author and review realistic evaluation tasks based on Clinical Study Reports, DSURs, PSURs/PBRERs ...

... writing thorough free-response answers with specific geographic examples. Adapts instruction using mapping activities, case study analysis, and AP-style practice to support students often taking ...

Research & Writing Attorney ALBUQUERQUE, NM No relocation required - Albuquerque-area and remote ... Experienced investigators (retired police officers), dedicated case managers, and paralegals.

Research & Writing Attorney ALBUQUERQUE, NM No relocation required - Albuquerque-area and remote ... Experienced investigators (retired police officers), dedicated case managers, and paralegals.

Remote micro1 is engaging Medical Writers / Clinical Document Authors to participate in a customer ... Author and review realistic evaluation tasks based on Clinical Study Reports, DSURs, PSURs/PBRERs ...

Remote micro1 is engaging Pharmacovigilance Experts to contribute their advanced drug safety ... Reconcile figures and case counts across report sections and data sources, identifying and ...

Remote micro1 is engaging Pharmacovigilance Experts to contribute their advanced drug safety ... Reconcile figures and case counts across report sections and data sources, identifying and ...

Biostatistician

Jackson, MS · Remote

$60 - $65/hr

Remote micro1 is engaging Biostatisticians to contribute their clinical statistics expertise to a ... Provide structured written rationales distinguishing true statistical errors from acceptable ...

Remote micro1 is engaging Biostatisticians to contribute their clinical statistics expertise to a ... Provide structured written rationales distinguishing true statistical errors from acceptable ...

Biostatistician

Jackson, MS · Remote

$60 - $100/hr

Remote micro1 is engaging Biostatisticians to contribute to a customer's advanced project in AI ... Demonstrated command of clinical study design, regulatory documentation, and observational research ...

Remote micro1 is engaging Biostatisticians to contribute to a customer's advanced project in AI ... Demonstrated command of clinical study design, regulatory documentation, and observational research ...

Russian Tutor

Starkville, MS · Remote

$18 - $40/hr

Skilled at teaching Cyrillic reading and writing, case system application, and aspect pair usage in ... academic study. * Effective Teaching Methods: Ability to identify concepts students commonly ...

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Remote Case Study Writer information

What is the difference between Remote Case Study Writer vs Remote Content Writer?

AspectRemote Case Study WriterRemote Content Writer
CredentialsWriting experience, industry knowledge, sometimes marketing or business backgroundGeneral writing skills, SEO knowledge, content marketing experience
Work EnvironmentFreelance or remote, often project-based, working with businesses or agenciesRemote, creating various content types like blogs, articles, social media posts
Industry UsageCommon in consulting, B2B, tech, healthcare sectorsUsed across multiple industries including marketing, media, education

The main difference is that Remote Case Study Writers focus on creating detailed, industry-specific case studies that showcase client success stories, requiring specialized knowledge. Remote Content Writers produce a broader range of content types for various purposes. Both roles are remote and require strong writing skills, but their focus and output differ significantly.

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For Remote Case Study Writer jobs in Mississippi, the most frequently searched job titles are:

What job categories do people searching Remote Case Study Writer jobs in Mississippi look for?

The top searched job categories for Remote Case Study Writer jobs in Mississippi are:

What cities in Mississippi are hiring for Remote Case Study Writer jobs?

Cities in Mississippi with the most Remote Case Study Writer job openings:

Medical Writer / Clinical Document Author

Jackson, MS • Remote

micro1 AI
Software Development • 11 - 50 employees

$50 - $80/hr

Part-time

This job post has expired 1 day ago. Applications are no longer accepted.


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.