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41268 - Assoc Medical Data Review Mgr

Iqvia
IQVIA
0-3 years
Not Disclosed
10 Jan. 22, 2026
Job Description
Job Type: Full Time Education: B.Sc/M.Sc/M.Pharma/B.Pharma/Life Sciences Skills: Causality Assessment, Clinical SAS Programming, Communication Skills, CPC Certified, GCP guidelines, ICD-10 CM Codes, CPT-Codes, HCPCS Codes, ICD-10 CM, CPT, HCPCS Coding, ICH guidelines, ICSR Case Processing, Interpersonal Skill, Labelling Assessment, MedDRA Coding, Medical Billing, Medical Coding, Medical Terminology, Narrative Writing, Research & Development, Technical Skill, Triage of ICSRs, WHO DD Coding

Associate Medical Data Review Manager

Location: Bangalore, India
Job Type: Full-Time
Application Deadline: February 4, 2026
Experience Required: 0–3 years (MBBS/MD)
Job ID: R1523546


Company Overview

IQVIA is a global leader in clinical research services, healthcare intelligence, and life sciences solutions. We accelerate the development and commercialization of innovative medical treatments by leveraging advanced analytics, technology, and domain expertise. Our teams provide high-quality data management, medical review, and clinical trial support to ensure patient safety and regulatory compliance worldwide.


Role Overview

The Associate Medical Data Review Manager (AMDRM) provides medical review expertise to ensure clinical trial data is accurate, medically consistent, and meets regulatory and client standards. This role also provides project management support to optimize workflows, improve data quality, and support study teams in clinical data sciences.


Key Responsibilities

  • Review clinical trial data for medical plausibility and patient anomalies per protocol.

  • Provide project management support including workload projections, continuous process improvements, and issue escalation.

  • Maintain strong relationships with internal teams, key decision makers, and clients.

  • Track service performance, identify root causes of issues, and implement remedial actions.

  • Serve as a Subject Matter Expert (SME) in medical data review processes.

  • Continuously identify opportunities to improve efficiency and quality of deliverables.

  • Provide therapeutic area or indication-specific training to project clinical teams.

  • Attend project kick-off meetings, team meetings, and client meetings as required.


Qualifications & Experience

  • Education: MBBS with 2+ years of experience, or MD with any experience; freshers considered.

  • Professional Skills:

    • Experience in clinical data sciences at a CRO, pharmaceutical company, or medical environment.

    • Strong understanding of clinical and medical data.

    • Knowledge of medical terminology, pharmacology, anatomy, and physiology.

    • Operational focus with ability to monitor metrics and take corrective actions.

    • Excellent communication, interpersonal, and teamwork skills.

    • Strong organizational, problem-solving, and project management skills.

    • Ability to work on multiple projects with minimal supervision.

    • Customer-focused with ability to build and maintain strong relationships.


Why Join IQVIA

  • Gain global exposure in clinical data review and medical data sciences.

  • Work on impactful clinical research projects in collaboration with expert teams.

  • Opportunities for professional development, mentorship, and career growth.

  • Contribute to the delivery of high-quality data management solutions that support patient safety and regulatory compliance.


Apply Now via thepharmadaily.com to join IQVIA as an Associate Medical Data Review Manager and take your career in clinical data sciences to the next level.