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Associate Central Monitoring Specialist

Novo Nordisk
10+ years
INR 30 LPA – 40 LPA
Bangalore, India
1 June 19, 2026
Job Description
Job Type: Hybrid Education: B.Sc/M.Sc/M.Pharma/B.Pharma/Life Sciences Skills: ICH guidelines, ICSR Case Processing, Labelling Assessment, MedDRA Coding, mRS and EQ-5D-5L, Triage of ICSRs, WHO DD Coding

Associate Central Monitoring Specialist

Department: Clinical Development
Team: Centralized Monitoring Unit (CMU), Clinical Drug Development
Location: Bangalore, Karnataka, India
Employment Type: Full-Time
Work Mode: Hybrid / On-Site

Role Summary

The Associate Central Monitoring Specialist serves as a Subject Matter Expert (SME) within the Centralized Monitoring Unit (CMU), driving the execution of Risk-Based Quality Management (RBQM) and centralized monitoring activities across global clinical studies.

This role combines clinical trial operations expertise, advanced data analytics, risk identification, process leadership, and stakeholder management to ensure patient safety, data integrity, protocol compliance, and operational excellence. The position requires deep knowledge of centralized monitoring methodologies, risk-based monitoring frameworks, audit readiness, and clinical trial oversight within a global pharmaceutical environment.

Key Responsibilities

Central Monitoring & RBQM Execution

  • Act as a Subject Matter Expert (SME) for:

    • Centralized Monitoring

    • Risk-Based Quality Management (RBQM)

    • Clinical Trial Risk Oversight

  • Perform centralized monitoring activities utilizing:

    • Dashboards

    • Data Visualization Platforms

    • Analytics Tools

    • Novo Nordisk Clinical Systems

  • Support development, implementation, and monitoring of:

    • Key Risk Indicators (KRIs)

    • Risk Assessment Frameworks

    • Study Oversight Strategies

  • Ensure proactive identification and management of study risks.

Risk Identification & Data Analytics

  • Analyze aggregate clinical trial data to identify:

    • Emerging Risks

    • Data Trends

    • Protocol Deviations

    • Compliance Issues

    • Operational Inefficiencies

  • Investigate unusual data patterns and anomalies.

  • Interpret complex datasets to support informed decision-making.

  • Escalate critical risks and issues through appropriate governance channels.

  • Support root cause investigations and implementation of mitigation strategies.

Project Leadership & Operational Delivery

  • Lead or support complex monitoring projects and strategic workstreams.

  • Apply structured project management methodologies to ensure:

    • Timely Deliverables

    • High-Quality Outputs

    • Stakeholder Alignment

  • Track project milestones, risks, and dependencies.

  • Drive execution excellence across monitoring initiatives.

Process Standardization & Governance

  • Ensure consistency and standardization of central monitoring processes.

  • Own and maintain:

    • Standard Operating Procedures (SOPs)

    • Work Instructions

    • Guidance Documents

    • Process Documentation

  • Align processes with Novo Nordisk Process Management Framework standards.

  • Identify opportunities for process optimization and operational efficiency.

Cross-Functional Collaboration

  • Collaborate closely with:

    • RBQM Specialists

    • Clinical Research Managers (CRMs)

    • Clinical Research Associates (CRAs)

    • Trial Managers

    • Data Managers

    • Functional Programmers

    • Business Analysts

  • Serve as a key liaison between:

    • Centralized Monitoring Unit (CMU)

    • RBQM Office

    • Clinical Development Functions

  • Facilitate effective communication and alignment across global teams.

Audit, Inspection & Compliance Management

  • Lead audit and inspection readiness activities for Central Monitoring.

  • Represent CMU processes during:

    • Internal Audits

    • Regulatory Inspections

    • Compliance Reviews

  • Drive:

    • CAPA Development

    • CAPA Implementation

    • CAPA Closure Activities

  • Ensure compliance with:

    • ICH-GCP Guidelines

    • GxP Requirements

    • Regulatory Expectations

    • Internal Quality Standards

Mentorship & Knowledge Sharing

  • Mentor and support less experienced team members.

  • Contribute to:

    • Onboarding Programs

    • Training Materials

    • Knowledge Management Initiatives

  • Promote a culture of continuous learning and collaboration.

  • Share best practices across monitoring teams and stakeholders.

Innovation & Continuous Improvement

  • Identify opportunities to improve monitoring efficiency through:

    • Automation

    • Data Analytics

    • Advanced Visualization Tools

    • Digital Solutions

  • Support innovation initiatives that enhance RBQM capabilities.

  • Contribute to the continuous evolution of centralized monitoring practices.

Required Qualifications

Education

  • Bachelor's Degree in:

    • Life Sciences

    • Pharmacy

    • Biotechnology

    • Nursing

    • Public Health

    • Medical Sciences

    • Related Scientific or Healthcare Discipline

Experience

  • Minimum 10+ years of experience in the pharmaceutical, biotechnology, or clinical research industry.

  • Strong experience in:

    • Clinical Trial Operations

    • Centralized Monitoring

    • Risk-Based Quality Management (RBQM)

    • Clinical Study Oversight

  • Experience applying RBQM methodologies across global clinical studies.

  • Proven experience managing complex projects and workstreams independently.