Thursday, January 8, 2026
HomeJobsApply Now for Medical Data reviewer Manager Role at IQVIA

Apply Now for Medical Data reviewer Manager Role at IQVIA

IQVIA Careers: Apply Now for Medical Data Reviewer Manager Role

IQVIA Careers: IQVIA offers a compelling opportunity for qualified medical professionals to take on a critical leadership role as an Associate Medical Data Review Manager. This position is ideal for MBBS or MD professionals with experience in clinical data sciences who are looking to combine medical expertise with data integrity, analytics, and project management. Based in Bengaluru or Thane (hybrid), this role supports global clinical studies and contributes directly to improving patient outcomes through high-quality clinical data.

IQVIA Careers: Job Details

  • Position: Associate Medical Data Review Manager
  • Location: Bengaluru / Thane, India
  • Work Mode: Hybrid
  • Employment Type: Full-Time

About IQVIA

IQVIA is a global leader in clinical research services, healthcare intelligence, and commercial insights for the life sciences industry. Operating in over 100 countries with approximately 88,000 employees, IQVIA combines deep domain expertise with advanced analytics, Healthcare-grade AI™, and high-quality health data. The organization is committed to accelerating the development and commercialization of innovative medical treatments while maintaining the highest standards of patient privacy, data security, and regulatory compliance.

IQVIA Careers: Qualifications

  • MBBS or MD with at least 2+ years of relevant work experience
  • Experience in clinical data sciences within a CRO, pharmaceutical company, or medical environment
  • Strong understanding of medical terminology, pharmacology, anatomy, and physiology
  • Proven leadership and project management capabilities
  • Ability to work independently in a matrix team environment

About the Role

The Associate Medical Data Review Manager serves as a Subject Level Data Reviewer (SLDR) and provides medical, clinical, and scientific oversight to ensure data quality and integrity across clinical studies. The role involves identifying anomalies in patient-reported data, supporting audit readiness, and acting as a subject matter expert across multidisciplinary teams.

Key Responsibilities

  • Perform subject-level data review to identify and resolve data anomalies
  • Conduct in-stream data trend analysis for protocol compliance and data integrity
  • Drive end-to-end study data quality and audit readiness
  • Provide medical and scientific advisory support to study teams
  • Act as a clinical data scientist by reviewing visual analytics and presenting findings
  • Define data capture requirements aligned with protocol and reporting needs
  • Maintain strong customer relationships and ensure timely issue resolution
  • Serve as SME and Point of Contact (POC) or backup POC

CLICK HERE TO APPLY

RELATED ARTICLES

LEAVE A REPLY

Please enter your comment!
Please enter your name here

Most Popular

Recent Comments