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Assoc Medical Data Review Mgr

IQVIA
2+ years
₹8 – ₹14 LPA
15 Aug. 6, 2026
Job Description
Job Type: Full Time, Hybrid, Remote Education: B.Sc./ M.Sc./ M.Pharm/ B.Pharm/ Life Sciences Skills:

Associate Medical Data Review Manager

Company: IQVIA
Job Title: Associate Medical Data Review Manager
Job ID: R1554443
Job Type: Full-time
Location: Bengaluru, Karnataka, India
Work Model: Hybrid


Experience Required

  • MBBS: Minimum 2+ years of experience preferred.

  • MD: Freshers may be considered.

  • Experience in clinical data sciences, medical review, CRO, pharmaceutical, or healthcare environments is preferred.


Educational Qualification

Candidates should possess:

  • MBBS (Bachelor of Medicine, Bachelor of Surgery) with relevant experience
    OR

  • MD (Doctor of Medicine) with any level of experience


Department

Clinical Data Sciences / Medical Data Review / Clinical Research


Job Summary

IQVIA is hiring an Associate Medical Data Review Manager to provide medical review expertise and support high-quality clinical data management activities. The role focuses on reviewing structured patient data from a clinical perspective, identifying medical inconsistencies, ensuring data accuracy, supporting clinical study teams, and improving the quality of clinical research deliverables.

The selected candidate will work closely with clinical teams, project managers, clients, and internal stakeholders to ensure medical data quality, compliance, and operational excellence.


Key Responsibilities

  • Perform medical review of clinical trial patient data.

  • Identify patient anomalies and evaluate medical plausibility according to study protocols.

  • Review clinical data for medical consistency and accuracy.

  • Provide project management support for clinical data review activities.

  • Collaborate with clinical study teams and key stakeholders.

  • Support continuous process improvement initiatives.

  • Manage issue escalation and resolution activities.

  • Monitor service performance and identify root causes of quality issues.

  • Ensure timely resolution of compliance-related concerns.

  • Act as a Subject Matter Expert (SME) for medical data review activities.

  • Provide therapeutic area and indication-based training to clinical teams.

  • Participate in:

    • Study kick-off meetings

    • Weekly project meetings

    • Client meetings

  • Improve efficiency and quality of medical data review processes.


Required Skills

  • Medical Data Review

  • Clinical Data Sciences

  • Clinical Research

  • Medical Terminology

  • Pharmacology

  • Anatomy and Physiology

  • Patient Data Review

  • Clinical Trial Data Analysis

  • Medical Coding Understanding

  • Data Quality Management

  • Compliance Monitoring

  • Project Management

  • Root Cause Analysis

  • Process Improvement

  • Team Leadership

  • Client Communication

  • Problem-Solving Skills


Preferred Qualifications

  • Experience working in:

    • Clinical Research Organizations (CROs)

    • Pharmaceutical companies

    • Healthcare environments

  • Strong understanding of clinical and medical data.

  • Ability to interpret patient-level clinical information.

  • Knowledge of clinical trial processes and protocols.

  • Experience managing multiple projects and priorities.

  • Strong leadership and coaching abilities.


Roles and Responsibilities

  • Work independently with minimal supervision.

  • Provide medical expertise for clinical data review projects.

  • Manage operational metrics and project status information.

  • Identify issues and recommend corrective actions.

  • Maintain strong relationships with clients and internal teams.

  • Ensure delivery of accurate, high-quality medical data products.


Work Environment

  • Full-time employment.

  • Hybrid work model.

  • Collaboration with global clinical research teams.

  • Opportunity to work on pharmaceutical and healthcare projects.


About IQVIA

IQVIA is a global leader in clinical research services, healthcare intelligence, and life sciences technology solutions. The company supports pharmaceutical, biotechnology, and healthcare organizations by combining advanced analytics, technology, and clinical expertise to accelerate the development of innovative medical treatments.


Estimated Salary Package

The official job posting does not disclose the salary. Based on market trends for Medical Data Review roles in Bengaluru:

Experience

Estimated Annual CTC

MBBS + 2–3 years

₹8 – ₹14 LPA

MD Fresher

₹10 – ₹18 LPA

MD with experience

₹15 – ₹25 LPA

Expected Average CTC: ₹10–18 LPA, depending on medical qualification (MBBS/MD), clinical research experience, leadership skills, and IQVIA's compensation structure.


Who Should Apply

Candidates with:

  • MBBS with 2+ years of relevant experience.

  • MD qualification (freshers can apply).

  • Knowledge of clinical research and medical data review.

  • Understanding of pharmacology, anatomy, and physiology.

  • Strong analytical and communication skills.

  • Ability to work with clinical teams and manage multiple priorities.


Location

  • Bengaluru, Karnataka, India


Employment Type

  • Full-time

  • Hybrid Work Model


Key Highlights

  • Opportunity to work in global clinical research and medical data operations.

  • Direct involvement in clinical trial data quality and patient safety.

  • Exposure to medical review, clinical data sciences, and therapeutic areas.

  • Opportunity to work as a medical subject matter expert.

  • Hybrid work flexibility.

  • Career growth opportunities within IQVIA's global healthcare ecosystem.