Senior / Regulatory Affairs Consultant - Advertising and Promotion

🌍 Remote, USA 🎯 Full-time πŸ• Posted Recently

Job Description

We are seeking a motivated

Senior / Regulatory Affairs Consultant – Advertising & Promotion to join Parexel and work as a trusted partner within a major client engagement. In this role, you will partner with cross-functional teams to ensure that all promotional, marketing, educational, and social media materials comply with US regulatory requirements. You’ll play a key role in supporting product launches, campaigns, and ongoing promotional activities while safeguarding compliance and patient trust.

Key Responsibilities β€’ Review and approve advertising and promotional materials, including direct-to-consumer campaigns, medical education, and social media content. β€’ Provide regulatory guidance to cross-functional teams (Marketing, Medical Affairs, Legal) during promotional material development. β€’ Participate in promotional review committees, ensuring alignment with FDA regulations and company standards. β€’ Collaborate with global teams to ensure consistency across markets while meeting US-specific requirements.

β€’ Maintain compliance with FDA 21 CFR Part 202 and other relevant US regulations. β€’ Support preparation of responses to regulatory inquiries related to promotional activities. β€’ Track and manage promotional submissions and approvals in regulatory systems β€’ Manage SOPs and electronic review systems. Qualifications β€’ Education: Bachelor’s degree in Life Sciences, Pharmacy, Regulatory Affairs, or related field. Experience: β€’ 3–5 years of pharmaceutical/biotech related industry experience. β€’ Direct experience in advertising and promotional regulatory review.

β€’ Familiarity with FDA regulations governing promotional materials. Skills: β€’ Strong organizational skills with the ability to manage multiple projects under tight timelines. β€’ Excellent communication skills, with the ability to explain regulatory concepts, including FDA regulations/guidances, clearly to cross-functional partners. β€’ Attention to detail combined with strategic thinking. β€’ Proficiency with bolthires Office and regulatory systems (e.g., Veeva PromoMats, eDMS). β€’ Ability to create and revise Ad/Promo SOPs to ensure promotional materials are updated as required by FDA regulations and company standards.

Competencies: β€’ Knowledge of US regulatory requirements for advertising and promotion. β€’ Demonstrated problem-solving ability and sound decision-making. β€’ Ability to work effectively in a matrix environment and collaborate across diverse teams. β€’ Strong interpersonal skills with cross-cultural awareness. β€’ Fluency in English (verbal and written). #LI-LB1 #LI-REMOTE Apply tot his job

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