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Document control specialist Jobs in Louisville, KY

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Document control specialist • louisville ky

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Remote Medical Writer / Clinical Document Author

Micro1Shively, Kentucky, US
$50.00 hourly
Remote
Full-time

Medical Writer / Clinical Document Author.AI data lab for training frontier models and evaluating AI agents.Experts contribute their diverse subject matter knowledge across domains such as finance,... Show more

Remote Medical Writer / Clinical Document Author

Micro1New Albany, Indiana, US
$50.00 hourly
Remote
Full-time

Medical Writer / Clinical Document Author.AI data lab for training frontier models and evaluating AI agents.Experts contribute their diverse subject matter knowledge across domains such as finance,... Show more

Inventory Control Analyst

Apply now!Louisville, United States, KY
Full-time

Arvato is an innovative and leading global 3PL service provider in supply chain management and e-commerce.With 20,000 team members at over 100 locations, we focus on the Consumer Products, Tech, He... Show more

Senior Insurance Loss Control Consultant

Alexander & SchmidtJeffersonville, IN, USA
Full-time

Senior Insurance Loss Control Consultant.At Alexander & Schmidt, a Senior Insurance Loss Control Consultant performs inspections and prepares in-depth reports for insurance underwriting purposes.In... Show more

Quality Control Supervisor

SU SolutionsLouisville, KY, US
Full-time
Quick Apply

We are seeking a dedicated and detail-oriented Quality Control Supervisor (Fabrication) to join our team in Louisville, KY.In this role, you will play a crucial part in ensuring that our fabricatio... Show more

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Senior Insurance Loss Control Consultant

Alexander & Schmidt - Getting the Job Done as a Trusted and Reliable PartnerJeffersonville, IN, United States
Full-time

Senior Insurance Loss Control Consultant.At Alexander & Schmidt, a Senior Insurance Loss Control Consultant performs inspections and prepares in-depth reports for insurance underwriting purposes.In... Show more

Associate Manager, Control

Yum BrandsLouisville, KY, United States
$99,200.00 yearly
Full-time

Ready to make your mark at an iconic global powerhouse? Join Yum! Brands - the parent company behind KFC, Pizza Hut, Taco Bell and Habit Burger & Grill - be a part of our reinvention for Greater Gr... Show more

QA/QC Protection & Control Engineer 2

GAI ConsultantsLouisville, KY , US
Full-time

GAI is seeking a highly skilled and experienced QA/QC Protection & Control Engineer 2 to oversee QA/QC on design, development, and implementation of protection and control systems for high-voltage ... Show more

Merchandising Specialist

Premium Retail ServicesJeffersonville, IN, United States
Full-time

Join Premium Retail Services as a Merchandising Specialist, where you'll bring top brands to life in stores across your community.Represent hundreds of beloved brands across multiple retail locatio... Show more

Quality Control Technician

KellyNew Albany, Indiana, US
$18.00 hourly
Temporary

Hours: Monday- Friday 7am-3:30pm.As an Quality Technician, you will be responsible for performing visual inspections, verifying dimensions, and ensuring the quality of parts and processes.You ... Show more

Inventory Control Specialist

Tennant CompanyLouisville, KY, US
Full-time

With more than $1B in revenue, Tennant Company is a globally recognized leader in the cleaning equipment industry.For the past 150 years, we have been passionate about developing and manufacturing ... Show more

Control Systems Engineer

Beneficial Talent SourceLouisville, KY, United States
$105,000.00 yearly
Full-time

We’re Hiring: Control Systems Engineer – Louisville, KY.Citizens or Green Card holders only.Are you passionate about automation and fluid process controls? This is your chance to design... Show more

Infection Control Employee Health Nurse

Kindred Hospital Louisville at Jewish HospitalLouisville, KY
Full-time

We value every voice by caring deeply for every patient and each other.We show courage by running toward the challenge and we lean into new ideas by embracing curiosity and question asking.Together... Show more

Receipting Specialist

Summit Fire & SecurityLouisville, KY, United States
Full-time

The purpose of the Receipting Specialist position is to process all vendor invoices, shipping statements, and account for internal stock issues into the internal database.Perform processing of vend... Show more

Inventory Control Clerk

ArvatoLouisville, United States
Full-time

This role partners closely with warehouse and operations teams, utilizing SAP and RF systems to support daily inventory control activities and drive continuous improvement.Use the RF system &#... Show more

Seasonal Pest Control Technician

Mira HomeLouisville, Kentucky, United States, 40202
$18.00 hourly
Full-time
Quick Apply

About Mira Home - Pest Control:.Our mission is simple: we worry about the bugs so our customers don’t have to.We pride ourselves on a culture of independence, safety, and exceptional service.Whethe... Show more

Senior Consultant, Risk Control - Equipment Breakdown

Liberty Mutual Insurance GroupLouisville, KY, United States
Full-time

Under limited supervision, we provide loss prevention consulting services within the Property and Marine Loss Prevention department, specializing in equipment breakdown risk.Completes Boiler and Pr... Show more

QA/QC Supervisor (Quality Assurance / Quality Control)

Eosol GroupLouisville, US
$82,000.00 yearly
Full-time

We're Hiring | QA/QC Supervisor (Quality Assurance / Quality Control) – Solar Project | Kentucky.EOSOL is looking for an experienced.QA/QC (Quality Assurance / Quality Control) Supervisor.We a... Show more

Louisville, KY - Loss Control Field Inspector – Independent Contractor

Associated Services InspectionsLouisville, Kentucky, United States
Full-time

Immediate openings available in your area!.Associated Services Inspections, Ltd.ASI delivers customized, high‑quality underwriting reports with fast turnaround times, supporting superior decision‑m... Show more

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Remote Medical Writer / Clinical Document Author

Remote Medical Writer / Clinical Document Author

Micro1Shively, Kentucky, US
2 days ago
Salary
$50.00 hourly
Job type
  • Full-time
  • Remote
Job description
Medical Writer / Clinical Document Author$50 - $80/hourpay

Required Skills

regulatory medical writingclinical study report authoringich e3 guidelinesscientific accuracy assessmentsource data verificationclinical protocol interpretationtfl (tables, figures, listings) analysiswritten communicationstructured feedback provisioncollaborative problem-solvingai-assisted documentation evaluationperiodic safety documentation (ich e2f, ich e2c)ectd (electronic common technical document) knowledgeoncology and haematology domain expertise

About micro1

micro1 is the leading AI data lab for training frontier models and evaluating AI agents. Experts contribute their diverse subject matter knowledge across domains such as finance, healthcare, STEM engineering, and more. micro1 transforms that real-world expertise into high-quality training data, evaluations, and feedback loops that improve how AI systems learn, reason, and perform.

Our platform identifies and vets top talent through an AI recruiter, enabling high-quality expert contributions at scale. We aim to enable 1 billion people to do meaningful work by applying their expertise to AI. As our global expert network grows, micro1 is building the human intelligence layer for frontier AI.

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.