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Medical Annotator Project Manager

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Onsite

Medical Annotator Project Manager

Shaip Ai Data (india)

Medical Annotator Project Manager

Skills

Google Cloud PlatformTesting & QAMachine LearningJiraAsanaCompliance

15 days ago

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Important information


Contract type:

Permanent

Location:

Ahmedabad, Gujarat, India

Work mode:

Onsite

Published on:

9 October 2026

What they need


Role Summary

You will lead our healthcare data team, delivering de-identification, pseudonymization, NER annotation, medical coding and medical imaging annotation projects. You will own delivery, quality, privacy compliance and client communication, and you will lead and mentor a team of medical annotators, coders and QA reviewers. This is a contract role for 12 months.

Key Responsibilities

  • Plan and run end-to-end annotation projects, covering scope, timelines, resourcing and delivery.
  • Lead, coach and performance-manage a team of 57 annotators, coders and QA reviewers.
  • Work with clients to turn clinical requirements into annotation guidelines and schemas, and keep those guidelines current.
  • Apply the right de-identification approach for each project (HIPAA Safe Harbor, HIPAA Expert Determination, or GDPR pseudonymization/anonymization) and make sure the team follows it.
  • Set and track quality metrics such as accuracy, inter-annotator agreement, turnaround time and rework rate. Run QA and feedback loops.
  • Provide clinical oversight on medical terminology, coding standards and edge cases.
  • Manage annotation tools and platforms, and coordinate with tech and ML teams.
  • Communicate and coordinate with vendors (annotation tool providers, staffing and outsourcing partners, and other third-party service providers) on scope, timelines, pricing, deliverables, quality and escalations, and track vendor performance against agreed SLAs.
  • Report project status, risks and escalations to management and clients on a regular schedule.
  • Handle tight deadlines, shifting priorities and client escalations calmly.

Requirements

Must Have

  • Education: A medical or allied-health degree: B.Pharm, or an equivalent such as Pharm.D, MBBS, BDS, BAMS, BHMS, BPT or B.Sc Nursing. Candidates from a non-medical background will not be considered. An MBA is preferred but not mandatory.
  • Clinical research experience: 3–5 years in clinical research or a related healthcare data field (CDM, pharmacovigilance, medical coding or similar).
  • Leadership experience: 3–5 years as a project lead, with demonstrated success leading a team of at least 5–7 people.
  • Privacy and compliance: Working knowledge of HIPAA (Privacy Rule, including the Safe Harbor method and its 18 identifiers, and the Expert Determination method) and GDPR (including pseudonymization vs. anonymization).
  • Medical knowledge: Strong grounding in medical terminology, clinical documentation and clinical data workflows.
  • Communication: Excellent written and verbal skills, including client-facing and vendor-facing experience.
  • Resilience: Proven ability to perform under pressure and manage multiple deadlines.
  • Location: Willingness to work from our Ahmedabad office.
  • Availability: Ability to join at short notice and commit to a 12 month contract.

Good to Have

  • Hands-on experience with de-identification, NER or other medical text or imaging annotation.
  • Familiarity with coding systems (ICD-10, MedDRA, WHODrug, SNOMED CT) and coding certifications (CPC, CCS or similar).
  • Knowledge of India's DPDP Act and ICH-GCP.
  • Experience with annotation tools (e.g., Label Studio, Labelbox, Encord, Prodigy) and project tools (Jira, Asana).

Key Competencies

Team leadership, clinical judgment, attention to detail, stakeholder and vendor management, problem-solving and accountability.

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