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Document processor Jobs in Columbia, SC

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Document processor • columbia sc

Last updated: 1 day ago

Remote Medical Writer / Clinical Document Author

Micro1West Columbia, South Carolina, 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 Word and PDF Experts

Micro1St. Andrews, South Carolina, US
$20.00 hourly
Remote
Full-time

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.AI... Show more

8-11 Business Analyst

Focused HR SolutionsColumbia, South Carolina, United States
$65.00–$80.00 hourly
Full-time
Quick Apply

Our direct client has an opening for a  Business Analyst 10964-1   .This position is up to 9 months, with the option of extension, and is in Columbia, SC.Corp to Corps are NOT allowe... Show more

Change Control, Continuous Improvement Manager

Nephron PharmaceuticalsWest Columbia, SC, United States
Full-time

Change Control Continuous Improvement Manager.The Change Control Continuous Improvement Manager is responsible for identifying, developing, and implementing process improvement initiatives within t... Show more

Remote Role || Business Analyst - Advanced || Columbia, SC

InstantServe LLCColumbia, SC, United States
Temporary

Location: Columbia, SC Type: 12-month contract.The Client is seeking an experienced Business Analyst to support the Information Technology Services Project Management Office (PMO) in analyzing busi... Show more

Technical Writer (RFP Specialist) - Contract - Columbia, SC

SUNSHINE ENTERPRISE USA LLCColumbia, SC, us
Full-time
Quick Apply

Technical Writer (RFP Specialist).Columbia, SC Hybrid (4 days in office, 1 days remote).Candidate MUST be a SC resident or willing to relocate to SC prior to starting the role at their own expense.... Show more

Valuations Processor

Hansen Talent Group (HTG)West Columbia, SC, United States
Full-time

Hansen Talent Group is hiring a Valuations Processor for a financial services organization in Columbia SC.Research and monitor federal and state tax regulations related to retirement plan distribut... Show more

Manager, Document Management

The Nuclear CompanyColumbia, SC, United States
$150,000.00 yearly
Full-time

The Nuclear Company is the fastest growing startup in the nuclear and energy space creating a never before seen fleet-scale approach to building nuclear reactors.Through its design-once, build-many... Show more

Document Control Specialist

Scout MotorsColumbia, SC, United States
$95,000.00 yearly
Full-time

Join us at Scout Motors and be part of shaping the future of transportation.If you're ready to drive change and make history, apply now!.Become part of an iconic brand that is set to revolutionize ... Show more

Senior Consultant - WIC Business and Technology Consulting

MaximusColumbia, US
$105,000.00 yearly
Full-time

Essential Duties and Responsibilities: - Collaborate with project managers on various initiatives and projects to track progress and provide support as necessary.Support leadership in ensuri... Show more

Real Property Analyst (Contingent Upon Contract Award)

Anglin Consulting GroupColumbia, SC, USA
Full-time
Quick Apply

Real Property AnalystThis position is contingent upon contract award and funding.Employment will not commence unless and until the contract is awarded and funding is confirmed.Anglin Consulting Gro... Show more

Business Analyst Consultant / Technical Writer

IntersourcesColumbia, SC, United States
Full-time

Business Analyst Consultant / Technical Writer.Location: 1801 Main Street, Columbia, SC 29201.Work Arrangement: Hybrid 4 days onsite and 1 day remote.Interview Process: One virtual interview.Cand... Show more

Quality Assurance Analyst - Consultant

LancesoftColumbia, SC, US
Full-time
Quick Apply

IT - SCDHHS - Quality Assurance Analyst –Consultant.The Quality Assurance Analyst –Consultant is responsible for performing comprehensive testing of technical solutions to identify, iso... Show more

Business Analyst

Lumen Solutions Group Inc.Columbia, SC, United States
Temporary

Location: Columbia, SC (Hybrid) Contract: 12+ Months Contract.Job Description Required Skills and Experience.Minimum 1 year of experience in business analysis using IBM Cram software.Minimum 1 year... Show more

Senior Mortgage Underwriter (Remote)

First Citizens BankColumbia, SC, United States
$76,500.00 yearly
Full-time

This is a remote role that may be hired in several markets across the United States.Loan Underwriting - Documents and underwrites mortgage loans products.Gathers and reviews information pertaining ... Show more

Gatekeeper 2nd Shift

Fresh ExpressColumbia, SC, USA
Full-time
Quick Apply

Shift - 4:00pm - Until Finish The Gatekeeper is responsible for transporting finished pallets from the production line to the Lantech Machines utilizing an electric pallet jack, hand jack or forkli... Show more

Lot Assistant-Columbia SC

Associates Asset RecoveryColumbia, SC, US
Full-time
Quick Apply

Lot Assistant Job Description We are one of the largest repossession companies in the US.We have multiple locations throughout SC, NC and Georgia.We are looking for someone to come in and help assi... Show more

Program Coordinator I - 61062062 & 61093661

State of South CarolinaWest Columbia, SC, United States
Full-time

The SCDE Office of Health and Nutrition is seeking a motivated individual for the position of Program Coordinator I, with the United States Department of Agriculture (USDA) Food Distribution Progra... Show more

CNA - Residential/Med Tech

Lutheran Homes of South CarolinaColumbia, SC, United States
Full-time

Rice Estate - Columbia, SC 29203.Under the supervision of the Director of Nursing, the CNA/Med Tech provides direct care to residents, assisting with personal care, hygiene, mobility, and other dai... Show more

Insurance Defense Paralegal

GpacColumbia, South Carolina, United States
Full-time
Quick Apply

A respected and growing law firm is seeking an experienced.This role will assist attorneys with all phases of litigation, including case management, discovery, medical record review, document prepa... Show more

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Remote Medical Writer / Clinical Document Author

Remote Medical Writer / Clinical Document Author

Micro1West Columbia, South Carolina, US
6 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.