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Verantos

Real-world data curation for pharmacoepidemiology

Clinical Annotator

Clinical Support & Patient AdministrationConfirmed live in the last 24 hours
Full-timePune, Maharashtra, IndiaNo salary listedIn-person

About the Job

Requirements

  • A bachelor's degree or above in pharmacy, nursing, medicine, or social work.
  • At least one year of clinical experience in the field.
  • At least three years of work experience as a medical annotator.
  • Ability to work on multiple projects in a fast-paced environment.
  • Flexibility, initiative, professionalism, and ability to work under pressure with minimal supervision.

Responsibilities

  • Annotate medical documents using annotation tools.
  • Review medical documents for completeness.
  • Identify and report protected health information in annotated medical documents to maintain patient privacy.
  • Manage specialized annotation requests and tasks under changing guidelines and tight deadlines.
  • Assess metrics to improve productivity.
  • Report and document issues with annotation tools and annotated documents to the development team when necessary.
  • Provide feedback to improve the existing annotation tool and increase annotation throughput and quality.
  • Contribute to the enhancement of workflow processes.

About the Company

Verantos

Real-world data curation for pharmacoepidemiology

Verantos provides high-quality real-world data for pharmacoepidemiology, enhanced by careful curation and clinical-inference processes, plus agentic AI tools to generate valid evidence quickly and at lower cost. Its product stack collects and harmonizes real-world data, applies domain-specific curation and inference, and uses AI-assisted workflows to produce evidence for clinical development, comparative effectiveness, regulatory submissions, label expansion, safety assessments, and post-marketing commitments. Unlike traditional HEOR approaches, Verantos emphasizes data quality, structured interpretation, and scalable AI-driven evidence generation to accelerate decision-making. The company's goal is to enable faster, more accurate evidence generation that supports drug development, regulatory approval, and long-term safety monitoring while reducing time and expense.

Company size
51-200
Company stage
Grant
Total funding
$220K
Headquarters
Menlo Park, CA
Founded
2013

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