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    • Minimum of 1 year in ICSR case processing.
    • Good understanding of global and regional Pharmacovigilance regulations.
    • Should be flexible to work in Shifts.
    • Provide feedback and ongoing workshops to develop the medical reviewers.
    • Interaction with the clients medical team and clinical team.
    • Assesses factors that might affect subject/patient’s safety and clinical data integrity at an.
    • Any risks to protocol/GCP compliance, trial conduct, patient…
    • Qualification - MBBS or MD/MS ( Mandatory).
    • Minimum 1 year of ICSR (Individual Case Safety Report) experience.
    • Review diagnostic reports and validate that the correct category and subcategory are selected (e.g., CT-Abdomen, Ultrasound-Transvaginal).
    • Candidate should have 1+ years of relevant experience in pharmacovigilance.
    • Minimum of 1 year in ICSR case processing.
    • Should be flexible to work in Shifts.
    • Minimum of 1 year in ICSR case processing.
    • Good understanding of global and regional Pharmacovigilance regulations.
    • Should be flexible to work in Shifts.
    • Strong understanding of medical terminology and clinical trial processes.
    • The ideal candidate will be responsible for reviewing medical records, clinical…
    • Tracking and maintenance of medical enquiries.
    • Quality check of the medical enquires responses.
    • Ensures effective functioning of assigned projects in compliance…
  • View similar jobs with this employer
    • Process clinical data: Ensure accuracy and completeness of project data.
    • Contribution to healthcare: Play a vital role in ensuring reliable data that supports…
    • Strong data entry and documentation skills.
    • Ability to work with sensitive patient data and maintain confidentiality.
    • Night shift (US Time Zones).
    • Proficiency in MS Excel for data management and reporting.
    • Support QA processes to ensure data integrity and compliance.
    • Review medical records to validate AI-generated HEDIS abstractions.
    • Participate in training and calibration sessions to ensure reviewer consistency.
    • Assesses factors that might affect subject/patient’s safety and clinical data integrity at an.
    • Any risks to protocol/GCP compliance, trial conduct, patient…
    • Internal monitoring of the data and suggesting tactics to improve care and achieve practice goals.
    • Should be able to analyze patient data recorded in software…

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Job Post Details

Pharmacovigilance Medical Reviewer - job post

Enhanceplus Placements LLP
Bengaluru, Karnataka
₹25,00,000 - ₹34,00,000 a year

Job details

Pay

  • ₹25,00,000 - ₹34,00,000 a year

Job type

  • Full-time

Location

Bengaluru, Karnataka

Benefits

Pulled from the full job description

  • Provident Fund

Full job description

  • Minimum of 1 year in ICSR case processing.
  • Good understanding of global and regional Pharmacovigilance regulations.
  • Individual contribution role.
  • Should be flexible to work in Shifts.
  • No WFH, base location is Chennai & Bangalore.
  • Minimum of 1 year in ICSR case processing.
  • Good understanding of global and regional Pharmacovigilance regulations.
  • Individual contribution role.
  • Should be flexible to work in Shifts.
  • No WFH, base location is Chennai & Bangalore.

Pay: ₹2,500,000.00 - ₹3,400,000.00 per year

Benefits:

  • Provident Fund

Work Location: In person

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