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Assoc Medical Data Review Mgr

IQVIA
2+ years
INR 10-18LPA
Bangalore, India
10 June 16, 2026
Job Description
Job Type: Full Time, Hybrid Education: B.Sc./ M.Sc./ M.Pharm/ B.Pharm/ Life Sciences Skills: Causality Assessment, Clinical SAS Programming, Clinical Trials, Detail-Oriented, Drug Development, Lifesciences, Negotiation Skills, Regulatory Compliance, Communication Skills, CPC Certified, CPT, Data Analysis, Document Management, Life Science, Regulatory Compliance, Waterfall Model, GCP guidelines, HCPCS Level II, ICD-10-CM, ICD-10 CM Codes, CPT-Codes, HCPCS Codes, ICD-10 CM, CPT, HCPCS Coding, ICD-10-PCS, ICH guidelines, ICSR Case Processing, Interpersonal Skill, Labelling Assessment, MedDRA Coding, Medical Billing

Job Title

Medical Data Review Specialist / Associate Medical Data Review Manager

Experience Required

Eligible Candidates

  • MBBS + 2 Years Experience
    OR

  • MD (Any Specialty) – Fresher or Experienced

Preferred Background

  • Clinical Data Sciences

  • Medical Review

  • Pharmacovigilance

  • Clinical Research

  • CRO or Pharmaceutical Industry Experience


Education

Mandatory

  • MBBS

Preferred

  • MD (Any Specialty)


Job Overview

This role focuses on providing Medical Review expertise for clinical trial data to ensure patient safety, data quality, protocol compliance, and medical consistency.

The professional will work closely with:

  • Clinical Study Teams

  • Data Management Teams

  • Physicians

  • Sponsors

  • Clinical Operations Teams

The primary objective is to identify medical inconsistencies, review patient data, and ensure medically plausible and protocol-compliant clinical trial data.


Key Responsibilities

Medical Data Review

  • Review patient clinical trial data for:

    • Medical consistency

    • Clinical plausibility

    • Protocol compliance

  • Identify:

    • Data anomalies

    • Missing information

    • Inconsistencies

    • Potential medical risks


Patient Safety & Data Quality

  • Evaluate subject-level data from a clinician's perspective.

  • Ensure medical congruency across:

    • Adverse Events (AEs)

    • Medical History

    • Concomitant Medications

    • Laboratory Results

    • Vital Signs

  • Support patient safety monitoring activities.


Project Management

  • Work with:

    • Clinical Teams

    • Data Management Teams

    • Sponsors

    • Stakeholders

  • Manage:

    • Workload planning

    • Escalations

    • Process improvements

    • Issue resolution


Subject Matter Expertise

  • Serve as Medical Data Review SME.

  • Provide guidance to study teams.

  • Support clinical review strategies.


Process Improvement

  • Identify opportunities for:

    • Efficiency improvements

    • Quality enhancements

    • Risk reduction

  • Support continuous improvement initiatives.


Training & Knowledge Sharing

  • Conduct therapeutic area training.

  • Mentor and support project teams.

  • Share indication-specific medical knowledge.


Client & Stakeholder Interaction

  • Attend:

    • Project Kick-Off Meetings

    • Weekly Review Meetings

    • Sponsor Meetings

    • Client Discussions

  • Build and maintain strong client relationships.


Required Skills & Knowledge

Medical Knowledge

Strong Understanding Of:

  • Medical Terminology

  • Pharmacology

  • Human Anatomy

  • Physiology

  • Pathophysiology

  • Clinical Medicine


Clinical Research Knowledge

Good Understanding Of:

  • Clinical Trials

  • Clinical Data Management

  • Medical Monitoring Concepts

  • GCP Guidelines

  • Clinical Study Conduct


Medical Data Review Skills

  • Medical Data Analysis

  • Patient Profile Assessment

  • Clinical Data Interpretation

  • Medical Coding Awareness

  • Risk Identification


Project Management Skills

  • Stakeholder Management

  • Issue Escalation

  • Team Coordination

  • Resource Planning

  • Process Improvement


Soft Skills

  • Excellent Communication

  • Customer Focus

  • Leadership Skills

  • Problem Solving

  • Time Management

  • Analytical Thinking

  • Teamwork

  • Decision Making


Preferred Candidate Profile

Must Have

  • MBBS Degree

  • Strong Clinical Knowledge

  • Interest in Clinical Research

  • Analytical Skills

  • Communication Skills

Preferred

  • MD Degree

  • CRO Experience

  • Clinical Data Review Experience

  • Medical Monitoring Exposure

  • Clinical Data Sciences Experience