Welcome Back

Google icon Sign in with Google
OR
I agree to abide by Pharmadaily Terms of Service and its Privacy Policy

Create Account

Google icon Sign up with Google
OR
By signing up, you agree to our Terms of Service and Privacy Policy
Instagram
youtube
Facebook

Associate Medical Data Review Manager

Iqvia
IQVIA
3-7 years
preferred by company
Bengaluru, India
1 May 18, 2026
Job Description
Job Type: Full Time Education: B.Sc/M.Sc/M.Pharma/B.Pharma/Life Sciences Skills: ICSR Case Processing, Interpersonal Skill, Labelling Assessment, MedDRA Coding, Medical Billing, Medical Coding

Associate Medical Data Review Manager – Clinical Data Review Jobs in Bengaluru | Hybrid Clinical Research Opportunity | IQVIA

Location: Bengaluru, India
Company: IQVIA
Job Type: Full-Time
Work Mode: Hybrid
Department: Clinical Data Sciences / Medical Data Review / Clinical Research
Experience Required: 3–7+ years of relevant clinical practice, clinical research, or clinical data sciences experience
Job Reference ID: R1535680


About the Company

IQVIA is a globally recognized leader in clinical research services, healthcare intelligence, commercial analytics, and life sciences technology solutions. The organization partners with pharmaceutical, biotechnology, medical device, and healthcare companies to accelerate clinical development and improve patient outcomes through data-driven innovation.

This opportunity is ideal for professionals seeking careers in medical data review, clinical data sciences, patient safety review, clinical operations support, and medical project management.


Job Overview

IQVIA is hiring an Associate Medical Data Review Manager for its Bengaluru hybrid office. This opportunity is designed for healthcare and clinical research professionals with expertise in clinical data review, medical anomaly detection, protocol-based patient data assessment, clinical operations, and stakeholder coordination.

The selected candidate will support structured patient data review from a clinician’s perspective, ensuring medical consistency, protocol compliance, subject safety, data plausibility, and operational excellence across clinical studies.

This role is ideal for professionals looking to build leadership-focused careers in clinical data sciences, medical review, and clinical project oversight.


Key Responsibilities

Medical Data Review & Clinical Assessment

  • Review structured patient clinical data to ensure medical congruency, plausibility, and protocol compliance.
  • Identify patient-level anomalies, inconsistencies, and clinical data quality concerns.
  • Support subject safety review through medical interpretation of trial data.
  • Apply clinical judgment to evaluate protocol-driven patient data.

Clinical Project Management Support

  • Provide project management support across medical data review activities.
  • Coordinate with clinical study teams, internal stakeholders, and decision-makers to maintain project delivery timelines.
  • Support workload planning, issue management, and continuous process optimization.
  • Escalate critical medical or operational concerns when necessary.

Operational Excellence & Process Improvement

  • Track service performance metrics and operational quality indicators.
  • Identify root causes of workflow issues and implement corrective actions.
  • Drive continuous improvements in data review quality and delivery efficiency.
  • Ensure compliance issue follow-up and timely resolution.

Subject Matter Expertise

  • Act as a Subject Matter Expert (SME) for assigned therapeutic areas or clinical data review processes.
  • Provide therapeutic area and indication-based training to project teams.
  • Support knowledge transfer and medical review best practices.

Client & Stakeholder Management

  • Build and maintain strong client relationships.
  • Participate in:
    • Project kickoff meetings
    • Weekly operational meetings
    • Client review discussions
    • Cross-functional coordination meetings
  • Support customer-facing communication and issue resolution.

Required Qualifications

Educational Qualification
Candidates must meet one of the following:

  • MBBS (Preferred / Strongly Suitable)
  • Other medical qualification with 5-year professional degree
  • Bachelor’s degree in clinical / biological sciences with minimum 3 years of relevant experience
  • Equivalent combination of education and relevant clinical research experience

Required Experience

  • Experience in:
    • Clinical data sciences
    • Clinical research
    • Clinical practice
    • CRO / pharmaceutical / healthcare environment
  • Demonstrated exposure to:
    • Medical data review
    • Clinical protocol interpretation
    • Patient safety review
    • Clinical anomaly detection
    • Project coordination

Required Skills

  • Strong understanding of:
    • Clinical and medical data
    • Medical terminology
    • Pharmacology
    • Human anatomy
    • Physiology
    • Clinical trial workflows
  • Strong operational focus on:
    • Metrics
    • Status reporting
    • Issue management
    • Process execution
  • Excellent:
    • Communication skills
    • Stakeholder management
    • Customer relationship management
    • Problem-solving capabilities
    • Project coordination skills
    • Coaching and leadership skills
  • Ability to:
    • Work independently
    • Handle multiple projects simultaneously
    • Manage competing deadlines
    • Deliver in fast-paced clinical environments