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41268 - Assoc Medical Data Review Mgr

2+ years
Not Disclosed
10 Nov. 24, 2025
Job Description
Job Type: Full Time Hybrid Education: B.Sc./ M.Sc./ M.Pharm/ B.Pharm/ 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: Bengaluru, India | Full-Time | Hybrid
Job ID: R1509344
Additional Global Locations Available

Position Overview

The Associate Medical Data Review Manager provides specialized medical review expertise to support high-quality clinical data management deliverables. This role ensures the medical accuracy, consistency, and plausibility of patient data and contributes to project management activities from a clinical perspective. You will collaborate with cross-functional teams, drive continuous improvement, and support clinical study teams in delivering compliant and reliable data outputs.


Key Responsibilities

  • Evaluate patient data to identify anomalies and ensure medical plausibility and protocol alignment.

  • Provide project management support with minimal supervision, working closely with clinical study teams and internal stakeholders.

  • Contribute to continuous process improvement initiatives, including issue escalation, risk identification, and quality enhancement.

  • Build and maintain strong customer relationships and ensure consistent service delivery.

  • Track service performance metrics, identify root causes of issues, and support the implementation of corrective actions.

  • Ensure timely follow-up and resolution of compliance and data quality issues.

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

  • Conduct therapeutic area and indication-specific training for clinical teams.

  • Participate in project Kick-Off meetings, internal team meetings, and client discussions as required.

  • Proactively seek opportunities to enhance efficiency and accuracy of clinical data review deliverables.


Required Qualifications & Experience

  • MBBS with 2+ years of experience, or MD candidates with any level of experience, including freshers.

  • Experience in clinical data sciences within a CRO, pharmaceutical company, or relevant medical environment with demonstrated leadership.

  • Strong understanding of clinical and medical data.

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

  • Medical background combined with an operational mindset focused on metrics and performance improvement.

  • Excellent communication, customer service, interpersonal, and teamwork skills.

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

  • Ability to work independently with minimal supervision and manage multiple priorities.

  • Proven ability to maintain effective working relationships with cross-functional teams and clients.

  • Strong customer-focused approach and commitment to data quality.


About IQVIA

IQVIA is a global leader in clinical research services, advanced analytics, and healthcare intelligence. The company accelerates drug development and supports life sciences organizations worldwide through data-driven insights, technology, and operational excellence.


How to Apply

Click Apply Now to submit your application through the global IQVIA careers portal.