SR

Compliance and Oversight Lead Manager

SRG , , united kingdom Posted 21 Oct 2026 Closing: 20 Nov 2026
Permanent On-site Featured

Clinical Role Overview

The Compliance & Oversight Lead Manager is responsible for monitoring business processes, ensuring data quality and compliance, and supporting continuous improvement initiatives within the Global Labeling, Artwork & U.S. Advertising & Promotion (GLAAM) function. The role involves identifying trends, driving process improvements, supporting remediation activities, and providing guidance and support to internal stakeholders involved in labeling activities.

Key Responsibilities

Compliance, Process & Data Oversight

  • Generate GLAAM project line listings and reports to support effective portfolio and resource management.
  • Maintain GLAAM SharePoint pages and resources, including brand tracking, Global Labelling Lead (GLL) trackers, and therapeutic area lists.
  • Support labelling processes through the creation and maintenance of business cases, job aids, work instructions, and process documentation.
  • Conduct routine process and quality monitoring in line with agreed business plans and schedules.
  • Support Quality Event (QE) investigations and remediation activities as required.
  • Analyse regulatory and labelling system data to ensure accuracy, quality, and alignment with key business reports.
  • Work with Subject Matter Experts (SMEs) to investigate and resolve data discrepancies.
  • Monitor business process performance and identify trends, risks, and opportunities for improvement.
  • Coordinate departmental initiatives aimed at enhancing labelling and regulatory processes.
  • Support the implementation of process improvements and efficiency initiatives.
  • Provide data-driven insights and recommendations to project leaders and key stakeholders.

Required Qualifications

Education

  • Bachelor's Degree or equivalent experience.
  • Degree in Regulatory Affairs or related discipline desirable.

Experience

  • 3-8 years' experience within a global or multinational pharmaceutical environment.
  • Previous experience within Labelling and/or Regulatory Affairs preferred.
  • Ability to work independently and manage multiple priorities effectively.
  • Demonstrated project management and project coordination experience.
  • Proven track record of delivering high-quality work to agreed timelines.
  • Strong written and verbal communication skills.
  • Experience supporting continuous improvement initiatives is desirable.

Technical Skills

  • Strong project management, coordination, and facilitation skills.
  • Excellent verbal and written communication abilities.
  • Strong analytical and problem-solving capabilities.
  • Ability to manage medium-complexity projects and adapt to evolving business needs.
  • Experience analysing and manipulating data to support decision-making.
  • Ability to synthesise complex data and processes into clear conclusions and actionable insights.
  • Knowledge of communication, process design, and continuous improvement tools desirable.
  • Ability to evaluate, diagnose, and improve business processes and systems.
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Key Details
  • Date Posted: 21 Oct 2026
  • Location: , , united kingdom
  • Employment Type: Permanent
  • Workplace: On-site
  • Category: Legal, Management & Operations
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Employer Information
SR
SRG
Verified Healthcare Employer

Verified NHS trust or certified UK healthcare facility offering professional development and clinical governance.

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