Talent.com
Clinical Documentation Review Specialist

Clinical Documentation Review Specialist

Priority1 GroupBengaluru, Republic Of India, IN
4 days ago
Job description

Registered Nurse – Documentation & Compliance

Bengaluru, Karnataka, India (Full-time)

Priority1 Group

About Us

Priority1 Group is a leading outsourcing and business support company helping NDIS providers across Australia manage their operational, compliance, and administrative functions. We ensure accuracy, efficiency, and full compliance so providers can focus on what truly matters participant care.

We’re expanding our compliance team and looking for a dedicated Nurse with strong documentation and reporting skills to support our NDIS operations.

Roles & Responsibilities

  • Review and validate daily support worker notes for accuracy and compliance with NDIS standards.
  • Prepare and review incident reports and participant summaries.
  • Identify discrepancies in clinical documentation and ensure timely resolution.
  • Maintain accurate participant health, care, and incident records in shared systems.
  • Collaborate with the Australian operations and compliance teams for smooth coordination.
  • Assist in developing care plans, documentation templates, and reporting frameworks.
  • Support internal audits and NDIS compliance checks.
  • Maintain strict confidentiality and uphold data security standards.

Qualifications Required

  • Registered Nurse (RN).
  • Prior experience in clinical documentation, compliance, or administrative roles within healthcare.
  • Strong attention to detail and accuracy.
  • Excellent written and verbal communication skills.
  • Proficiency in Microsoft Office and documentation systems.
  • Ability to work independently and collaboratively in a cross-functional team.
  • Willing to learn.
  • Why Work With Us?

  • Join a growing organisation supporting Australia’s disability and healthcare sector.
  • Be part of a collaborative, supportive, and mission-driven environment.
  • Opportunity to upskill in NDIS compliance and quality management.
  • Flexible work culture and career development opportunities.
  • If you’re passionate about accurate documentation and want to make an impact in the NDIS space, we’d love to hear from you.
  • Create a job alert for this search

    Documentation Specialist • Bengaluru, Republic Of India, IN

    Related jobs
    • Promoted
    Oncology Reimbursement Specialist

    Oncology Reimbursement Specialist

    RISABengaluru, Republic Of India, IN
    Cancer patients face not just a disease, but a broken system where delays in treatment are.RISA Labs is changing that with our Business. Operating System as a Service (BOSS) - a powerful platform bu...Show moreLast updated: 14 days ago
    • Promoted
    Clinical Project Manager

    Clinical Project Manager

    Biocon BiologicsBengaluru, Karnataka, India
    Proactively manages clinical trials from start-up to closure with a focus on trial timelines, quality, budget, and vendor oversight. Leads selection of CRO and vendors including identification of po...Show moreLast updated: 30+ days ago
    • Promoted
    Regulatory Affairs Specialist - Peptides or Injectable

    Regulatory Affairs Specialist - Peptides or Injectable

    BioconBengaluru, Karnataka, India
    Formulation Regulatory Affairs - for Peptide products or Injectables.Level - Deputy Manager / Associate Manager.Formulation Regulatory Affairs for Peptide products or Injectables.Drafting controlled...Show moreLast updated: 29 days ago
    • Promoted
    Regulatory Documentation & Compliance Specialist

    Regulatory Documentation & Compliance Specialist

    Brainwave ScienceHosūr, Republic Of India, IN
    Regulatory Documentation & Compliance Specialist (FCC, CE, FDA, RoHS, Cybersecurity).With over a decade of research and innovation, the company has developed advanced cognitive assessment solutions...Show moreLast updated: 23 hours ago
    • Promoted
    Medical Documentation Specialist

    Medical Documentation Specialist

    HighPoints Technologies India (P) LtdBengaluru, Republic Of India, IN
    We are looking to hire experienced Sr.Medical Transcriptionists / Editors who can accurately transcribe and edit radiology and diagnostic reports, while maintaining the highest standards of quality...Show moreLast updated: 30+ days ago
    • Promoted
    Document Quality Reviewer II

    Document Quality Reviewer II

    ParexelBengaluru, Karnataka, India
    When our values align theres no limit to what we can achieve.At Parexel we all share the same goal - to improve the worlds health. From clinical trials to regulatory consulting and market access eve...Show moreLast updated: 8 days ago
    • Promoted
    Medical Affairs Documentation Specialist

    Medical Affairs Documentation Specialist

    Biocon BiologicsBengaluru, Republic Of India, IN
    Writing, editing, reviewing, formatting, publishing regulatory (clinical and post marketing) documents and dossier sections in a manner compliant with FDA, EMA, CDSCO, ICH, CONSORT guidelines and o...Show moreLast updated: 16 days ago
    • Promoted
    Analyst- Document Review

    Analyst- Document Review

    Moraebangalore, karnataka, in
    Morae Global seeks to find the best and the brightest people – those who understand what it takes to deliver top quality solutions for our clients. We are currently seeking Analyst in Document Revie...Show moreLast updated: 3 days ago
    • Promoted
    Regulatory Submission Specialist

    Regulatory Submission Specialist

    Biocon BiologicsBengaluru, Republic Of India, IN
    Strong understanding of eCTD, NeeS, and ICH guidelines.Familiarity with Regulatory systems and Publishing tools.Use publishing tools such as : Lorenz Docubridge, Ectd Validator, ISI Toolbox, Adobe A...Show moreLast updated: 30+ days ago
    • Promoted
    Formulation Regulatory Affairs Specialist

    Formulation Regulatory Affairs Specialist

    BioconBengaluru, Republic Of India, IN
    Formulation Regulatory Affairs - for Peptide products or Injectables.Level - Deputy Manager / Associate Manager.Formulation Regulatory Affairs for Peptide products or Injectables.Drafting controlled...Show moreLast updated: 29 days ago
    • Promoted
    Temporary contract - Document Review

    Temporary contract - Document Review

    MoraeBengaluru, Karnataka, India
    Job Roles and Responsibilities Job Duration - 1-2 Months (Can be extended) Responsibilities will include identifying, extracting, and validating key contractual data points.Reviewing and capturing...Show moreLast updated: 1 day ago
    • Promoted
    Pharmacovigilance Medical Review Specialist

    Pharmacovigilance Medical Review Specialist

    IndegeneBengaluru, Republic Of India, IN
    We are a technology-led healthcare solutions provider.We are driven by our purpose to enable healthcare organizations to be future ready. We offer accelerated, global growth opportunities for talent...Show moreLast updated: 1 day ago
    • Promoted
    Mortgage Document Review Analyst

    Mortgage Document Review Analyst

    FirstsourceBengaluru, Republic Of India, IN
    A RP Sanjiv Goenka Group company.Firstsource is a leading provider of customized Business Process Management (BPM) services. We are trusted custodians and long-term partners to 100+ leading brands w...Show moreLast updated: 15 days ago
    • Promoted
    Clinical Data Reviewer (Contract)

    Clinical Data Reviewer (Contract)

    TriomicsBengaluru, Republic Of India, IN
    Triomics is building the modern technology stack for oncology trial sites and investigators that unifies the workflows of clinical care and clinical research, moving the healthcare industry closer ...Show moreLast updated: 14 days ago
    • Promoted
    Senior Record Quality Reviewer

    Senior Record Quality Reviewer

    Getingebangalore district, karnataka, in
    This is a 6-month contractual role.To complete a review of service records ensuring information and documentation is completed as per requirements. Update Excel file noting Yes or No to compliance w...Show moreLast updated: 14 days ago
    • Promoted
    Senior Clinical Data Associate

    Senior Clinical Data Associate

    Precision For MedicineBengaluru, India
    The Senior Clinical Data Associate provides data management support and assistance in all aspects of the clinical trial data management process from study start up to post database lock for assigne...Show moreLast updated: 30+ days ago
    • Promoted
    Publishing Specialist

    Publishing Specialist

    Biocon BiologicsBengaluru, Karnataka, India
    Strong understanding of eCTD, NeeS, and ICH guidelines.Familiarity with Regulatory systems and Publishing tools.Use publishing tools such as : Lorenz Docubridge, Ectd Validator, ISI Toolbox, Adobe A...Show moreLast updated: 30+ days ago
    • Promoted
    Clinical Regulatory Writer

    Clinical Regulatory Writer

    Biocon BiologicsBengaluru, Republic Of India, IN
    Writing, editing, reviewing, formatting, publishing regulatory (clinical and post marketing) documents and dossier sections in a manner compliant with FDA, EMA, CDSCO, ICH, CONSORT guidelines and o...Show moreLast updated: 16 days ago