Associate Director, Global Regulatory Advertising and Promotion

IQVIA

Associate Director ensuring compliance with advertising regulations at IQVIA. Collaborating with cross-functional teams to develop promotional materials and strategies that meet regulatory standards.

Posted 7/18/2026full-timeDurham • New Jersey, North Carolina, Pennsylvania • 🇺🇸 United StatesSenior💰 $103,600 - $288,600 per yearWebsite

Core Competencies

Role fit

Core Competencies

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Demonstrates expertise in Regulatory Affairs with a focus on compliance for promotional materials in the pharmaceutical, biotech, or medical device industries. Proficient in preparing regulatory submissions and leading cross-functional discussions while ensuring adherence to applicable regulations and industry trends.

Highest-signal resume keywords

Regulatory Affairs ExperiencePromotional Material ComplianceRegulatory Submissions PreparationCross-Functional CollaborationStrong Communication Skills

ATS Keywords

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Applicant Tracking System Keywords

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Hard Skills

Regulatory CompliancePromotional Regulations KnowledgeAdvertising and Promotion ExpertiseRegulatory SubmissionsTraining Program DevelopmentMonitoring Enforcement ActionsIndustry Trends Analysis

Soft Skills

Strong Written CommunicationStrong Verbal Communication

Industry Keywords

Life SciencesPharmacyBiotechMedical DeviceDigital Media ComplianceSocial Media Compliance

About the role

Key responsibilities & impact

Ensuring compliance with regulatory requirements for promotional and non-promotional materials
Leading discussions for assigned products during the Promotional Material Review Team (PMRT)
Supporting interactions with regulatory authorities
Preparing regulatory submissions for promotional materials
Developing and delivering training programs on promotional regulations
Monitoring enforcement actions and industry trends

Requirements

What you’ll need

Bachelor’s degree in a relevant field (e.g., Life Sciences, Pharmacy, Regulatory Affairs, or a related discipline)
Minimum 5 years of experience in Regulatory Affairs
At least 2 years focused on advertising and promotion in the pharmaceutical, biotech, or medical device industry
Strong knowledge of applicable regulations and enforcement trends
Prior experience working with cross-functional review committees in a regulated environment
Familiarity with digital and social media promotional compliance is a plus
Strong written and verbal communication skills

Benefits

Comp & perks

Health insurance
Paid time off
Professional development opportunities
Retirement plans