Senior Medical Data Abstractor

2 weeks ago

Bengaluru, Karnataka, India Triomics Full time ₹ 9,00,000 - ₹ 12,00,000 per year

Part of the Oncology Clinical Team, working on building Oncology Data dictionaries, Curation/Abstraction SOPs etc.

Position Summary:

The Person navigates electronic medical record systems and other medical databases. This role involves reviewing clinical trial data for consistency, completeness, and compliance with study protocols and regulatory requirements. reviews medical records, and abstracts medical record data related to specified disease and project requirements.

Essential Job Functions:

Screening of cases for relevant clinical trials across various projects and/or disease subtypes.

Knowledge related to cancer trials is essential and required, including understanding their

inclusion and exclusion criteria.

Ability to use critical thinking to understand and abstract complex concepts.

Building of data libraries and liaising with multiple departments when project specific

requirements/needs arise.

Act as an oncology subject matter expert (SME) across all cancers, especially across liquid cancer types.

Access electronic data systems for review of medical records and enter specific data into

congruent electronic data systems.

Ability to understand the Inclusion, Exclusion criteria, adverse event, hospitalization data,

medications details and categorize the data accordingly.

Review project specific documents, as needed, to develop familiarity with project goals and with the Abstractor tasks in each project.

Ability to understand the diagnostic, pathology and other reports and obtain the exact

information required according to trial specific SOPs.

Use other resources as needed to gain the knowledge required to perform Abstractor work on new projects.

Share medical knowledge and project-specific procedural knowledge with other Data Abstractors as needed.

Respond promptly to queries issued by the Lead Data Abstractor, Operations Manager or other project personnel.

Conduct additional duties as assigned, including review of selected medical records to assess

eligibility for new project, performing second level reviews/QC review of medical records.

Qualification:

Minimum 3+ years experience across data abstraction or any patient treatment related data is desirable.

Oncology experience is preferable; familiarity with how cancer is treated from diagnosis through treatment and recovery and an understanding of cancer terminology, with a strong focus and knowledge on liquid tumors is essential.

Experience in clinical research or related fields, especially in oncology trials is preferred.

An advanced level of clinical knowledge associated with chronic disease states is required.

Experience in clinical research or reviewed medical data for clinical trials.

Certification done in clinical research or clinical data management.

Education:

B.Sc (Nursing), BDS, BAMS, BHMS, MDS, BPharm, MPharm

Skills and Abilities:

Language: Strong communication skills both written and verbal to work with multiple internal and external clients in a fast paced environment.

Reasoning: Ability to make independent judgments in abstracting medical data and the

knowledge of when to seek input from other staff.

Flexibility: Flexibility in coping with changing work assignments, changing project requirements, varying training meeting schedules, and database resources that may not always function optimally.

Computer: Ability to create and maintain documents using Microsoft office( word, excel, outlook and powerpoint).

  • HEDIS Abstractor and Overreader

    6 days ago

    Bengaluru, Karnataka, India agilon health Full time ₹ 9,00,000 - ₹ 12,00,000 per year

    Company:AHIPL Agilon Health India Private LimitedJob Posting Location:India_BangaloreJob Title:HEDIS Abstractor and OverreaderJob Description:Position Summary:The HEDIS Abstractor and Overreader is responsible for the HEDIS Medical Record Review (MRR) process which includes accurately reviewing and abstracting medical records to determine compliance with...

  • Data Curation SME

    2 weeks ago

    Bengaluru, Karnataka, India Triomics Full time ₹ 9,00,000 - ₹ 12,00,000 per year

    About Triomics: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 to the vision of Clinical Research as a Care Option. Our platform, which is based on our proprietary oncology-focused large language model (OncoLLM)...

  • Data Curation SME

    2 weeks ago

    Bengaluru, Karnataka, India Triomics Full time ₹ 9,00,000 - ₹ 12,00,000 per year

    Part of the Oncology Clinical Team, working on building and developing Oncology Data dictionaries, liquid tumor pipeline from scratch and SOP creation by acting as an SME for the liquid tumor portfolio, along with secondary duties of Curation/Abstraction etc. Position Summary: We are seeking a highly skilled and experienced Data Curation Subject Matter...

  • Senior medical biller/ senior medical coder

    7 days ago

    Bengaluru, Karnataka, India Orchestrate Medical Full time

    Job Title: Team Lead / Senior Medical Biller/ Senior Medical CoderLocation: Remote / BangaloreCompany: Dr New Med.com / Required: Minimum 7 yearsSpecialty Preferred: CardiologySoftware Expertise Preferred: Athena EHR & Next Gen HER is an added advantage. Job Summary:We are seeking a highly experienced and detail-oriented Medical Biller/Coder to join our...

  • Senior Medical Biller/ Senior Medical Coder

    1 week ago

    Bengaluru, Karnataka, India Orchestrate Medical Full time

    Job Title: Team Lead / Senior Medical Biller/ Senior Medical CoderLocation: Remote / BangaloreCompany: DrNewMed.com /   https://www.orchestratemedical.com/Experience Required: Minimum 7 yearsSpecialty Preferred: CardiologySoftware Expertise Preferred: Athena EHR & NextGen HER is an added advantage. Job Summary:We are seeking a highly experienced and...

  • Senior Medical Biller/ Senior Medical Coder

    7 days ago

    Bengaluru, Karnataka, India Orchestrate Medical Full time

    Job Title: Team Lead / Senior Medical Biller/ Senior Medical Coder Location: Remote / Bangalore Company: DrNewMed.com /    Experience Required: Minimum 7 years Specialty Preferred: Cardiology Software Expertise Preferred: Athena EHR & NextGen HER is an added advantage. Job Summary: We are seeking a highly experienced and detail-oriented Medical...

  • hedis analyst

    2 weeks ago

    Bengaluru, Karnataka, India Randstad Full time

    Position Summary:The HEDIS Abstractor and Overreader is responsible for the HEDIS Medical Record Review (MRR)process which includes accurately reviewing and abstracting medical records to determinecompliance with HEDIS measure specifications, as well as conducting overreads to ensure dataquality, consistency and adherence to NCQA guidelines. This role will...

  • Diligent Medical Data Analyst

    1 week ago

    Bengaluru, Karnataka, India beBeeMedicalReviewer Full time ₹ 1,50,000 - ₹ 28,00,000

    Job OverviewWe are seeking a diligent and meticulous individual to fill the role of Trainee Medical Reviewer. The selected candidate will be responsible for reviewing medical records for accuracy and completeness.ResponsibilitiesReview medical records meticulously to ensure data integrity.Compile comprehensive reports based on medical data, providing...

  • Medical Data Specialist

    2 weeks ago

    Bengaluru, Karnataka, India beBeeMedical Full time ₹ 8,00,000 - ₹ 11,50,000

    Job Title: Medical Data SpecialistWe are seeking a skilled Medical Data Specialist to join our team. As a key member of our clinical drug development team, you will be responsible for conducting comprehensive medical reviews of clinical trial data across various therapy areas.The ideal candidate will have a graduate degree in Medicine and relevant experience...

  • Trainee - Medical Reviewer

    2 weeks ago

    Bengaluru, Karnataka, India Omega Healthcare Full time

    Job DescriptionKey Responsibilities:- Review and assess medical documents, including clinical trial data, safety reports, and regulatory submissions, for accuracy, consistency, and compliance with industry standards.- Assist in the preparation of regulatory documents, such as clinical study reports, informed consent forms, and patient safety reports.- Ensure...