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Associate Director, Global Study Lead

Gsk Plc
GSK plc
7+ years
Not Disclosed
Bangalore, India
10 May 14, 2026
Job Description
Job Type: Full Time Education: B.Sc./ M.Sc./ M.Pharm/ B.Pharm/ Life Sciences Skills: ICH guidelines, ICSR Case Processing, Interpersonal Skill, Labelling Assessment, MedDRA Coding, Medical Billing, Medical Coding, Medical Terminology, mRS and EQ-5D-5L., Narrative Writing, Research & Development, Technical Skill, Triage of ICSRs, WHO DD Coding

Associate Director, Global Study Lead

Job Details

  • Company: GSK (GlaxoSmithKline)

  • Role: Associate Director, Global Study Lead (GSL)

  • Location: Bengaluru, India

  • Site: Bengaluru Luxor North Tower

  • Department: Medical & Clinical

  • Job ID: 439886

  • Posted Date: 07 May 2026


Position Summary

The Associate Director, Global Study Lead (GSL) is responsible for leading the operational strategy, planning, execution, and end-to-end delivery of global clinical studies from study initiation through study closure and archiving.

The role serves as a key member of the Study Leadership Team (SLT), partnering with Clinical Leads and Study Statisticians to ensure studies are delivered on:

  • Time

  • Quality

  • Budget

  • Regulatory compliance

  • Scientific standards

The GSL acts as the Clinical Operations representative and drives cross-functional collaboration across global matrix teams.


Key Responsibilities

Strategic Study Leadership & Delivery

  • Lead operational strategy and execution for global clinical studies.

  • Ensure studies are delivered according to:

    • Timelines

    • Budget

    • Scientific standards

    • Company expectations

  • Conduct:

    • Study feasibility assessments

    • Governance preparation

    • Operational planning

  • Understand study contribution to broader clinical development programs and submissions.

  • Participate as a core member of the Study Leadership Team (SLT).


Operational Oversight, Risk & Issue Management

  • Provide end-to-end oversight to:

    • Global Study Managers (GSMs)

    • Study Managers (SMs)

  • Serve as escalation point for:

    • Clinical Operations

    • Vendors

    • Working groups

  • Identify, assess, and mitigate study risks proactively.

  • Ensure timely issue resolution while balancing risk and study objectives.


Compliance, Quality & Inspection Readiness

  • Ensure compliance with:

    • ICH/GCP guidelines

    • Global regulations

    • GSK SOPs

  • Oversee:

    • Protocol compliance

    • Quality management

    • Inspection readiness

  • Provide operational input into:

    • Protocols

    • Informed Consent Forms (ICFs)

    • Key study documents


Stakeholder Communication & Matrix Leadership

  • Build and lead cross-functional matrix teams.

  • Ensure effective communication of:

    • Study status

    • Risks

    • Timelines

    • Expectations

  • Collaborate with:

    • Clinical Operations Asset Lead (COAL)

    • Functional teams

    • Leadership stakeholders

  • Drive process improvement and operational excellence initiatives.


Financial & Vendor Management

  • Manage study budgets and financial reviews.

  • Lead:

    • Vendor assessment

    • Vendor selection

    • Vendor oversight

  • Monitor performance of:

    • CROs

    • FSO partners

    • External vendors

  • Act as escalation point for vendor delivery issues.


Innovation & Digital Transformation

  • Drive innovative clinical trial approaches including:

    • Decentralized Clinical Trials (DCTs)

    • Adaptive study models

  • Promote:

    • AI/ML adoption

    • Automation

    • Digital clinical tools

  • Improve operational efficiency and study delivery processes.


Required Qualifications

Educational Qualification

  • Degree in:

    • Life Sciences

    • Health Informatics

    • Related healthcare/science field

  • Or equivalent industry experience.


Experience Requirements

  • Extensive clinical development experience.

  • Proven experience in operational study delivery within:

    • Pharmaceutical industry

    • CRO environment

  • Experience leading:

    • Global studies

    • Multi-country clinical trials

    • Cross-functional matrix teams

  • Strong understanding of:

    • ICH/GCP

    • Global regulatory requirements

  • Experience in:

    • Stakeholder management

    • Budget management

    • Risk mitigation

    • Project delivery


Preferred Qualifications

Preferred Experience

  • Therapeutic area expertise across specific indications.

  • Experience with:

    • Adaptive trial designs

    • Decentralized Clinical Trials (DCTs)

    • Platform, umbrella, or basket trials

  • Strong CRO/vendor management experience.

  • Experience leading:

    • Change management

    • Innovation initiatives

    • Process modernization


Key Skills Required

  • Global clinical study management

  • Clinical operations leadership

  • Risk management

  • Vendor management

  • Matrix team leadership

  • Stakeholder engagement

  • Budget & financial management

  • Strategic planning

  • Regulatory compliance

  • Decision-making & problem-solving

  • Communication & collaboration

  • AI/ML and digital clinical operations awareness


GSK Core Values

Candidates are expected to demonstrate:

  • Patient Focus

  • Transparency

  • Respect

  • Integrity

  • Courage

  • Accountability

  • Teamwork

  • Continuous Learning


About GSK

GSK is a global biopharma company focused on uniting science, technology, and talent to get ahead of disease together. The company works across key therapeutic areas including:

  • Oncology

  • HIV

  • Respiratory

  • Immunology & Inflammation

  • Infectious Diseases

GSK aims to positively impact the health of 2.5 billion people globally through innovation in medicines and vaccines.


Important Notes

  • GSK does not charge any recruitment or interview fee.

  • Candidates should only trust emails ending with “@gsk.com”.

  • Suspicious recruitment activities should be reported to:


Recruitment Support

For recruitment adjustments or accessibility support: