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
2-5 years
INR 10 LPA – 18 LPA
Bangalore, India
1 June 17, 2026
Job Description
Job Type: Full Time Education: MBBS/MD Skills: Communication Skills, CPC Certified, CPT, Data Analysis, Document Management, Life Science, Regulatory Compliance, Waterfall Model, GCP guidelines, HCPCS Level II, ICD-10-CM

Associate Medical Data Review Manager

Location: Bangalore, India
Employment Type: Full Time


Job Overview

The Associate Medical Data Review Manager is responsible for providing medical review expertise and clinical data oversight to ensure high-quality clinical data management deliverables. The role focuses on structured patient data review from a clinician's perspective, identifying patient-level anomalies, ensuring medical plausibility of clinical data, supporting project management activities, and collaborating with cross-functional teams to improve study quality and efficiency.

This position combines clinical expertise, medical data analysis, stakeholder management, and operational leadership within a clinical research environment.


Key Responsibilities

Medical Data Review

  • Review patient-level clinical trial data to ensure medical consistency and protocol compliance.

  • Identify patient anomalies and medically implausible data points.

  • Evaluate clinical data for accuracy, completeness, and medical congruency.

  • Assess patient safety and clinical relevance of findings.

  • Escalate significant medical findings and data issues to appropriate stakeholders.

  • Ensure quality and integrity of medical review deliverables.

Project Management & Clinical Support

  • Provide project management support to clinical study teams.

  • Collaborate with:

    • Clinical Operations Teams

    • Data Management Teams

    • Medical Monitors

    • Sponsors

    • Internal Functional Groups

  • Support workload planning, issue tracking, and project execution activities.

  • Participate in process improvement and operational excellence initiatives.

  • Assist with risk identification and mitigation planning.

Subject Matter Expertise

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

  • Provide clinical guidance and recommendations to project teams.

  • Support resolution of medical data review issues.

  • Deliver therapeutic area and indication-specific training to study teams.

  • Share best practices and lessons learned across projects.

Quality & Compliance

  • Ensure compliance with:

    • Study Protocols

    • Clinical Data Review Standards

    • Regulatory Requirements

    • Internal SOPs

  • Monitor service performance and support corrective action implementation.

  • Ensure timely resolution of compliance-related issues.

  • Support inspection readiness and quality improvement initiatives.

Client & Stakeholder Management

  • Maintain strong relationships with internal and external stakeholders.

  • Participate in:

    • Kick-Off Meetings (KOMs)

    • Weekly Study Meetings

    • Client Meetings

    • Project Review Meetings

  • Communicate findings, recommendations, and project updates effectively.

  • Provide customer-focused support and issue resolution.

Continuous Improvement

  • Identify opportunities to improve quality, efficiency, and consistency of deliverables.

  • Support process enhancement initiatives and operational improvements.

  • Contribute to development of best practices and standard methodologies.

  • Assist in mentoring and coaching team members when required.


Qualifications

Education

  • MBBS (Bachelor of Medicine and Bachelor of Surgery)

OR

  • Other Medical Degree with a 5-year professional qualification

OR

  • Bachelor's Degree in:

    • Clinical Sciences

    • Biological Sciences

    • Life Sciences

    • Related Healthcare Discipline

    with a minimum of 3 years of clinical practice or clinical research experience.

  • Equivalent combination of education, skills, and experience may be considered.


Experience (Minimum Required)

  • Experience within:

    • Clinical Research Organizations (CROs)

    • Pharmaceutical Industry

    • Clinical Data Sciences

    • Medical Review Functions

    • Clinical Practice

  • Demonstrated leadership or project coordination experience.

Clinical Knowledge

  • Strong understanding of:

    • Clinical Trial Processes

    • Clinical Data Review

    • Medical Terminology

    • Pharmacology

    • Anatomy

    • Physiology

Professional Skills

  • Strong project management capabilities.

  • Excellent organizational and prioritization skills.

  • Strong analytical and problem-solving abilities.

  • Ability to manage multiple projects simultaneously.

  • Excellent communication and stakeholder management skills.

  • Ability to work independently with minimal supervision.

  • Strong customer-service orientation.