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Associate Medical Reviewer

Novo Nordisk
1-2 years
Not Disclosed
Bangalore, India
2 June 5, 2026
Job Description
Job Type: Full Time Education: MBBS/MD Skills: gmp knowledge, HSE Knowledge , Logistics and Transportation Management, Master Data, Operational Excellence, Sap Erp, supply chain management, Supply Planning, Warehouse Management, ICD-10 CM Codes, CPT-Codes, HCPCS Codes, ICD-10 CM, CPT, HCPCS Coding, ICH guidelines, ICSR Case Processing

Associate Medical Reviewer

Department: Clinical Development – Central Monitoring Unit (CMU)
Location: Bangalore, Karnataka, India
Employment Type: Full-Time
Experience Required: 1–2 Years
Education: MBBS + MD
Industry: Pharmaceutical / Biotechnology / Clinical Research


Position Overview

We are seeking a highly motivated and detail-oriented Associate Medical Reviewer to join the Central Monitoring Unit (CMU). The successful candidate will play a critical role in ensuring patient safety, protocol compliance, and data quality across global clinical trials.

As an Associate Medical Reviewer, you will conduct comprehensive medical reviews of clinical trial data, identify potential safety concerns and data inconsistencies, collaborate with clinical trial stakeholders, and support medical monitoring activities throughout the study lifecycle.

This role offers an opportunity to work closely with Medical Specialists, Data Managers, Trial Managers, and cross-functional clinical development teams while contributing to the successful execution of clinical trials and the development of innovative therapies.


Key Responsibilities

Medical Data Review & Monitoring

  • Conduct detailed medical reviews of assigned clinical trial subjects to ensure data quality, consistency, and accuracy.

  • Evaluate clinical trial data for medical relevance, completeness, and protocol compliance.

  • Monitor patient safety throughout the clinical trial lifecycle.

  • Identify clinically significant findings, outliers, trends, and safety concerns requiring further investigation.

  • Assess adverse events, laboratory data, concomitant medications, and medical histories for consistency and accuracy.

  • Ensure compliance with study protocols, Good Clinical Practice (GCP), ICH Guidelines, local regulations, and company SOPs.


Medical Issue Resolution

  • Identify medical inconsistencies, discrepancies, and protocol deviations within clinical trial data.

  • Collaborate with investigational site personnel, healthcare professionals, and study teams to resolve data queries.

  • Escalate significant medical concerns and safety findings to Medical Specialists when appropriate.

  • Support root cause analysis and corrective actions for recurring data quality issues.


Clinical Trial Monitoring Support

  • Perform medical monitoring activities to support centralized monitoring efforts.

  • Conduct protocol compliance assessments across study sites.

  • Review clinically significant outliers and abnormal data patterns.

  • Support medical data cleaning activities and quality review processes.

  • Contribute to risk-based monitoring activities and centralized monitoring initiatives.


Stakeholder Collaboration

  • Present medical review findings and recommendations to Medical Specialists and study teams.

  • Collaborate closely with:

    • Medical Specialists

    • Data Managers

    • Trial Managers

    • Clinical Operations Teams

    • Central Monitoring Teams

    • Investigational Site Staff

  • Participate in discussions supporting clinical decision-making and study quality improvements.

  • Maintain effective communication with internal and external stakeholders.


Documentation & Compliance

  • Maintain accurate and complete documentation of all medical review activities.

  • Ensure inspection readiness and audit preparedness at all times.

  • Maintain records in accordance with regulatory requirements and internal procedures.

  • Contribute to quality assurance and compliance initiatives.


Continuous Learning & Knowledge Development

  • Stay current with:

    • Therapeutic area knowledge

    • Protocol-specific requirements

    • Medical and scientific developments

    • Clinical trial regulations and guidelines

  • Participate in training programs and professional development initiatives.

  • Contribute to knowledge sharing and best practice implementation within the team.


Required Qualifications

Education

Mandatory Qualification

  • MBBS (Bachelor of Medicine, Bachelor of Surgery)

AND

  • MD (Doctor of Medicine) in a relevant medical specialty