GSK Hiring for Central Monitoring Lead Role

ByPharma Hiring Hub

GlaxoSmithKline (GSK), a global biopharmaceutical leader, is hiring for the role of Central Monitoring Lead at its Bengaluru location. This position is ideal for professionals looking to advance their careers in clinical research, centralized monitoring, and Risk‑Based Quality Management (RBQM).

The role focuses on clinical trial data analytics, centralized monitoring strategies, and quality oversight, supporting proactive risk identification and data‑driven decision‑making across global clinical studies. Candidates will work closely with cross‑functional teams to ensure trial quality, patient safety, and regulatory compliance.

This is a high‑impact opportunity for experienced professionals seeking to work within a global biopharma environment, contributing to modern, analytics‑driven clinical trial execution at GSK.

GSk career

Job Overview

  • Position: Central Monitoring Lead
  • Department: Clinical research
  • Location: Bengaluru, India
  • Experience: 1 to 3 Years
  • Qualification: B.Pharm, M.pharm
  • Job Type: Full-Time
  • Last Date to apply: 8 April 2026

Key Responsibilities – Central Monitoring Lead Role

  • RBQM Leadership & Accountability: Serve as the single point of accountability for embedding Risk‑Based Quality Management (RBQM) across assigned GSK‑sponsored and outsourced studies, aligned with study protocols, GSK SOPs, ICH‑GCP, and regulatory requirements.
  • Lead the setup and execution of Central Monitoring and data analytics tools at the study level.
  • Cross‑Functional Risk Planning: Drive strategic discussions with Global Clinical Operations, Data Strategy & Management, Biostatistics & Programming, Medical, and Safety teams (CSI) to define critical‑to‑quality (CTQ) measures and prevent study risks or failures.
  • Risk Assessment & Mitigation Strategy: Initiate and lead multifunctional teams to identify critical clinical and data processes supporting robust risk assessment and development of effective mitigation strategies.
  • Monitoring Strategy Execution: Ensure study and data‑related risk mitigations are fit for purpose and incorporated into key operational documents such as:
    • Monitoring Plans
    • Central Monitoring Plans
    • Quality Tolerance Limit (QTL) Reports
  • Data Analytics & Vendor Oversight: Maintain accountability for study‑level data analytics investigations, vendor deliverables, and ongoing performance monitoring.
  • Central Monitoring Oversight: Assess and implement central monitoring requirements at the study level, ensuring a consistent approach to data quality oversight across multiple studies.
  • Signal Interpretation & Issue Management: Interpret analytic signals during trial execution and assess their impact on study quality and participant safety.
  • Work closely with central monitors and study teams to investigate and resolve data trends, signals, and emerging issues.
  • RBQM & Central Monitoring Subject Matter Expertise: Act as a Subject Matter Expert (SME) for RBQM and Centralized Monitoring, supporting both central and local study teams.
  • Training & Mentorship: Mentor and train new CMDA members and study teams on RBQM principles, centralized monitoring processes, and RBQM tools, applying the 70‑20‑10 learning model.

Required Skills & Qualifications

  • Central Monitoring Experience: 1–3 years of experience in centralized monitoring within drug development or clinical research environments.
  • RBQM & Data Analytics Expertise: Hands‑on experience with RBQM tools and data analytics, with a clear understanding of their impact on data integrity and trial quality.
  • Clinical Development Knowledge: End‑to‑end clinical development experience, including exposure to clinical trial execution and oversight.
  • Quality, Risk & Compliance Knowledge
    • Strong understanding of quality, safety, risk management, and compliance principles, aligned with ICH and GCP requirements.
    • Ability to work in compliance with GSK R&D policies and SOPs.
  • Data Interpretation Skills: Good understanding of graphics and data visualizations, with the ability to interpret trends and derive meaningful insights from analytical outputs.
  • Communication & Analytical Skills
    • Fluent in English (written and spoken).
    • Excellent communication, influencing, and analytical skills to support cross‑functional decision‑making.

Why Join GSK?

  • Flexible Working Model: Benefit from Performance with Choice, offering a hybrid work model (2–3 days per week in the office) along with flexible working hours to support work‑life balance.
  • Global Pharmaceutical Organization: Be part of a well‑established, international biopharmaceutical company with a strong global presence and long‑term stability.
  • High‑Impact Role: Work with a professional team that plays a critical role in maintaining and strengthening GSK’s product portfolio across global markets.
  • Global Standards & Processes: Gain experience working with globally applied GSK standards, documentation practices, and quality frameworks.
  • Comprehensive Employee Benefits
    • Access a wide range of benefits, including:
    • Medical Insurance Plan
    • Life Insurance
    • Employee Retirement Program
    • Sports and Recreation Cards
    • Recreation Allowance
    • Annual Performance Bonus
  • Supportive Work Environment: Join a collaborative, supportive, and friendly workplace that encourages teamwork, growth, and professional development.

How to Apply

Interested candidates should apply only through the official company career website using the link provided below.

Apply Here

Important Disclaimer

This job post is shared for informational purposes only, based on publicly available job details. Candidates are advised to verify eligibility, job responsibilities, and application procedures from the official IQVIA website before applying.

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FAQ-Central Monitoring Lead Role

1. Who can apply for the Central Monitoring Lead role at GSK?

Professionals with 1–3 years of experience in centralized monitoring, RBQM, and data analytics within clinical development are eligible to apply.

2. What is the primary focus of this role?

The role focuses on Risk‑Based Quality Management (RBQM), centralized monitoring, data analytics, and quality oversight for GSK‑sponsored and outsourced clinical studies.

3. Does this role involve end‑to‑end clinical development activities?

Yes. The position requires end‑to‑end clinical development exposure, including study planning, execution, risk identification, and oversight through close‑out.

4. Will I work with cross‑functional teams?

Yes. You will collaborate closely with Clinical Operations, Data Strategy & Management, Biostatistics & Programming, Medical, Safety, and Central Monitoring teams.

5. Is experience with RBQM and data analytics mandatory?

Yes. Hands‑on experience with RBQM tools and data analytics, and the ability to interpret trends and signals impacting data integrity and study quality, is required.

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