Instagram
youtube
Facebook

Associate Director, Regulatory Affairs (Labeling) - Fsp

2-10 years
Not Disclosed
10 Nov. 26, 2025
Job Description
Job Type: Full Time Education: B.Sc/M.Sc/M.Pharma/B.Pharma/Life Sciences Skills: Causality Assessment, Clinical SAS Programming, Communication Skills, CPC Certified, GCP guidelines, ICD-10 CM Codes, CPT-Codes, HCPCS Codes, ICD-10 CM, CPT, HCPCS Coding, ICH guidelines, ICSR Case Processing, Interpersonal Skill, Labelling Assessment, MedDRA Coding, Medical Billing, Medical Coding, Medical Terminology, Narrative Writing, Research & Development, Technical Skill, Triage of ICSRs, WHO DD Coding

Associate Director, Regulatory Affairs (Labeling) – FSP

Location: Remote (North Carolina, United States)
Job ID: R-01335789
Employment Type: Full-Time
Category: Clinical Research


About the Role

Thermo Fisher Scientific is recruiting an Associate Director, Regulatory Affairs (Labeling) to support global labeling strategy, development, and lifecycle management across foundational and dependent markets. This fully remote position is part of the PPD® clinical research services division and contributes to bringing critical therapies to market through regulatory, scientific, and operational expertise.

The role requires deep knowledge of global labeling regulations, strong leadership capability, and demonstrated experience managing complex labeling operations within a large, matrixed environment.


Position Purpose

The Associate Director will oversee global labeling activities, ensuring compliance with regulatory standards across the U.S., EU, CH, DE, AU, and other key markets. This includes strategy development, end-to-end labeling execution, promotional and non-promotional material review, and regulatory documentation support.

This position acts as a key labeling strategist within Global Regulatory Affairs (GRA) and drives alignment between regulatory requirements, company objectives, and commercial strategies.


Key Responsibilities

Global Labeling Coordination and Management

  • Lead end-to-end labeling development for foundational and dependent markets.

  • Manage readability testing, translations, and linguistic reviews for EU/CH/DE markets.

  • Maintain and update CCDS, USPI, SmPC, and related core labeling documents.

  • Oversee preparation, submission, and upload of approved labels to internal and external systems (Documentum, Weblabel, Trackwise, Veeva, HA, ePIL).

  • Dispatch CCDS and foundational labels to partner markets and stakeholders.

  • Conduct labeling record maintenance and ensure accuracy across regulatory systems.

Governance and Compliance

  • Prepare documentation for Labeling Review Committee (LRC) and Global Labeling Committee (GLC).

  • Manage global labeling compliance, including FDA-508, quality control, and annual FDA drug listing/NDC requirements.

  • Support creation of DLS, CCDS, and regulatory labeling content.

  • Lead exception management and deviation reporting for foundational and non-foundational markets.

  • Ensure adherence to country-specific labeling regulations and artwork approval processes.

Regulatory and Cross-Functional Support

  • Manage Health Authority requests, RFIs, and labeling negotiations.

  • Provide regulatory guidance to Medical Affairs, Legal, Supply Chain, Commercial, and other cross-functional teams.

  • Review promotional and non-promotional materials for compliance with approved labeling.

  • Maintain SOPs and electronic review systems related to labeling and promotional review.

  • Provide strategic insights for therapeutic area teams and contribute to competitive intelligence.

Clinical Trial Regulatory Responsibilities

  • Develop CTA submission strategies across global markets.

  • Support compliance with EU CTR and other regional clinical trial regulations.

  • Serve as regulatory liaison between labeling, clinical operations, and global health authorities.

Operational and Administrative Activities

  • Maintain multi-market manuscripts and master artwork.

  • Manage administrative labeling updates for EU and global markets.

  • Lead annual strain update labeling activities for seasonal markets.

  • Participate in GRA strategic meetings and global labeling leadership updates.


Required Qualifications and Experience

Experience Requirements

  • Minimum 10+ years in the biotech/pharmaceutical industry.

  • Minimum 2+ years of direct regulatory labeling experience.

  • Minimum 5+ years of management or team leadership experience.

  • Experience with global labeling lifecycle management across US, EU, DE, CH, AU.

  • Proven track record leading cross-functional or matrixed teams.

  • Experience reviewing scientific, regulatory, and technical documentation.

  • Familiarity with labeling for flu campaigns, pandemic products, and promotional review compliance.

  • CTA submission experience preferred.

Education Requirements

  • Bachelor’s degree in Life Sciences, Chemistry, Pharmaceutical Sciences, Engineering, or related field.

  • Advanced degree (MSc, PharmD, PhD) preferred.


Technical Skills

  • Proficiency with regulatory and document systems:

    • Veeva RIMS, Veeva Vault

    • Apollo, Docubridge

    • Trackwise (Change Control)

    • SharePoint, Adobe Acrobat, Microsoft Office

    • TVT, Promomats, GLAMS

  • Strong understanding of:

    • Structured Product Labeling (SPL)

    • FDA-508 compliance

    • Digital labeling and electronic submission requirements

    • Promotional review workflows and CTA submission platforms


Core Competencies

  • Ability to function as a labeling strategist within GRA.

  • Comprehensive knowledge of global regulatory frameworks governing labeling and drug development.

  • Strong organizational and analytical skills with the ability to manage multiple high-complexity projects.

  • Effective cross-functional leadership with excellent communication skills.

  • Ability to influence stakeholders and convey complex regulatory concepts clearly.

  • Fluent in written and verbal English; additional languages are an advantage.