Jobs · New Jersey

Senior Manager Regulatory Affairs Advertising and Promotion

Sanofi · Morristown, NJ · 1 mo ago
HybridFull-time
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. Not a heading. We have "About The Job" paragraph: we can treat as About the role section. We have "About Sanofi" paragraph: maybe part of About the role? Could be separate but not required heading. Probably include in About the role. We have "Main Responsibilities": list of duties. Use

  • . We have "About You" with Basic Qualifications, Work Experience Required, Knowledge, Skills And Equivalent Experience. We need sections: Requirements, Qualifications, Skills maybe. We have "Why Choose Us?" which includes benefits etc. Could map to Benefits section. We have compensation line: "All compensation will be determined commensurate with demonstrated experience." That's vague; we should not create Pay section because it's not specific. So omit Pay. Schedule: not mentioned, omit. Benefits: we have "Enjoy a thoughtful, well-crafted rewards package... wide range of health and wellbeing benefits including high-quality healthcare, prevention and wellness programs and at least 14 weeks’ gender-neutral parental leave." Also "Employees may be eligible to participate in Company employee benefit programs, and additional benefits information can be found here." That's enough for Benefits section. We also have other motivational paragraphs: "Bring the miracles of science..." etc. Could be part of Benefits or separate but we can include in Benefits as prose. We need to avoid boilerplate: EEO etc. Remove. We must preserve all substantive information; not invent. Let's craft sections:

    About the role

    As the Senior Manager, Regulatory Affairs Advertising and Promotion within our GRA Advertising and Promo Team, you will be responsible for conducting the independent review of advertising, promotional, communications and other materials, and help develop and implement regulatory strategies for promotion and advertising campaigns. Ready to get started? Join the engine of Sanofi’s mission — where deep immunoscience meets bold, AI-powered research. In R&D, you’ll drive breakthroughs that could turn the impossible into possible for millions. With some direction from the Therapeutic Area Head, will conduct the independent review of advertising, promotional, communications and other materials, and help develop and implement regulatory strategies for promotion and advertising campaigns, including serving as regulatory lead for product launches. As the product A&P expert, contribute to the development and implementation of regulatory strategies for labeling, product defense, and development projects. Serve as the primary liaison with FDA, for assigned products, on matters related to advertising and promotional compliance matters.

    About Sanofi: We’re an R&D-driven, AI-powered biopharma company committed to improving people’s lives and delivering compelling growth. Our deep understanding of the immune system – and innovative pipeline – enables us to invent medicines and vaccines that treat and protect millions of people around the world. Together, we chase the miracles of science to improve people’s lives.

    Location maybe include in a

    after About the role? Could add a short p:

    Location: Morristown, NJ / Cambridge, MA

    Then Responsibilities:

    Responsibilities

    • Identifies product-specific or therapeutic area A&P issues and works with other teams to propose and implement solutions.
    • Identifies different strategies for addressing issues; advises of risk/benefit of each and assists clients with making sound business decisions with the understanding of the potential risk/benefits with respect to intervening regulatory matters.
    • Oversees and bears responsibility for the successful implementation of regulatory strategic objectives and projects with minimal supervision.
    • Active participant and Regulatory representative on brand teams and Review Committees (RC) for commercial and medical materials, respectively.
    • Provides guidance and feedback to internal Sanofi constituencies (commercial groups, R&D) to maximize the competitive impact of product development as well as ultimate promotion, advertising, and reimbursement.
    • Provides input to the Global organization on domestic regulatory strategies for in-line products through life cycle management programs.
    • Contribute A&P expertise to the development of optimal labeling on new and supplemental new drug applications.
    • Provides product-specific Regulatory strategies to mitigate risk; works in conjunction with brand team management to provide advice and risk/benefit analysis to maximize value to stakeholders.
    • Performs other duties as assigned.
    Now Requirements/Qualifications/Skills. We have Basic Qualifications: Bachelor’s degree from an accredited four-year college or university; Science focus preferred, but not require (typo). Work Experience Required: 3+ Years experience within pharmaceutical or medical device advertising and promotional review. Successful track record with relevant regulatory experience. Dealt effectively with cross-functional groups, which may include Medical, Legal, Marketing etc. Knowledge, Skills And Equivalent Experience: list many items. We could combine into Requirements (education + experience) and Skills (knowledge, skills). Or we could have Requirements (education + experience) and Qualifications (maybe same). But we need to avoid thin sections. Let's make:

    Requirements

    • Bachelor’s degree from an accredited four-year college or university; Science focus preferred.
    • 3+ years experience within pharmaceutical or medical device advertising and promotional review.
    • Successful track record with relevant regulatory experience.
    • Experience dealing effectively with cross‑functional groups (Medical, Legal, Marketing, etc.).

    Skills

    • Knowledge and understanding of complex medical and scientific subject matter.
    • Ability to work well within cross‑functional teams.
    • Solid oral communication and writing skills.
    • Understanding of the U.S. pharmaceutical marketplace and familiarity with medical terminology.
    • Ability to analyze data from different sources to draw conclusions and choose appropriate actions or develop solutions.
    • Develops collaborative relationships to facilitate accomplishment of work goals.
    • Develops and proposes innovative solutions in work situations.
    • Shows ability to use appropriate interpersonal styles and techniques to gain acceptance of ideas or plans.
    • Can build collaborative internal networks to obtain cooperation.
    • Unquestionable ethics, professional integrity and personal values consistent with Sanofi values.
    • Ability to balance projects with day‑to‑day duties, ensuring participation from other members of the department as needed.
    • Ability to establish priorities and timelines to effectively manage workload.
    • Ability to multi‑task well.
    • Deals with people in an honest and forthright manner, representing information and data accurately.
    Now Benefits:

    Benefits

    • Thoughtful, well‑crafted rewards package recognizing contribution and amplifying impact.
    • Wide range of health and wellbeing benefits including high‑quality healthcare, prevention and wellness programs.
    • At least 14 weeks’ gender‑neutral parental leave.
    • Opportunities to grow talent and drive career through promotions or lateral moves, domestically or internationally.
    • Work at the forefront of drug discovery, harnessing cutting‑edge AI, data, and digital platforms.
    • Help improve the lives of millions globally by making drug development quicker and more effective.
    We might also include the "Bring the miracles of science..." paragraph as prose in Benefits. Could add a

    before list. Let's add a

    describing the mission: "Bring the miracles of science to life alongside a supportive, future‑focused team. Discover endless opportunities to grow your talent and drive your career, whether it’s through a promotion or lateral move, at home or internationally. Enjoy a thoughtful, well‑crafted rewards package that recognizes your contribution and amplifies your impact. Take good care of yourself and your family, with a wide range of health and wellbeing benefits including high-quality healthcare, prevention and wellness programs and at least 14 weeks’ gender-neutral parental leave. Be part of a pioneering biopharma company that engages patients early in drug development and uses their insights to design studies that reflect real‑world needs. Work at the forefront of drug discovery, harnessing cutting‑edge AI, data, and digital platforms to push the boundaries of science. Help improve the lives of millions of people globally by making drug development quicker and more effective." Then list maybe not needed; but we already have list. Could keep prose and then list specifics. We must not repeat info. The prose already includes many of the benefit points; we could just keep prose and not list. But we need to use

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            . We can decide to not create a list for benefits and just have prose. That's fine. Thus Benefits section:

            Benefits

            ...prose...

            Now we need to ensure we didn't include Pay or Schedule sections. We also need to include location maybe as a short p after About the role or before Responsibilities. Let's add a

            Location: Morristown, NJ / Cambridge, MA

            after About the role. Now check for any boilerplate: we removed EEO, #GD-SA etc. Also removed "All compensation will be determined commensurate with demonstrated experience." (we omitted). Also removed "Employees may be eligible to participate in Company employee benefit programs, and additional benefits information can be found here." (we omitted as it's generic). Might be considered benefit but it's vague; we omitted. Check that we preserved all substantive information: Let's verify. From posting: - About The Job paragraph: we included. - About Sanofi paragraph: we included. - Main Responsibilities list: we included all items. - About You: Basic Qualifications: Bachelor’s degree... Science focus preferred, but not require (we captured). Work Experience Required: 3+ Years experience within pharmaceutical or medical device advertising and promotional review. Successful track record with relevant regulatory experience. Dealt effectively with cross-functional groups, which may include Medical, Legal, Marketing etc. (we captured). - Knowledge, Skills And Equivalent Experience: we captured all bullet points (converted to list). Let's verify each: Original list: - Knowledge and understanding of complex medical and scientific subject matter. - Ability to work well within cross-functional teams. - Demonstrates solid oral communication and writing skills. - Understanding of the U.S. pharmaceutical marketplace, and familiarity with medical terminology. - Understands issues, problems and opportunities by comparing data from different sources to draw conclusions and then can choose a course of action or develop the appropriate solution. - Develops collaborative relationships to facilitate the accomplishment of work goals. - Develops and proposes innovative solutions in work situations, trying different and novel ways to deal with work problems and opportunities. - Shows ability to use appropriate interpersonal styles and techniques to gain acceptance of ideas or plans. - Can build collaborative internal networks to obtain cooperation. - Unquestionable ethics, professional integrity and personal values consistent with the Sanofi values. - Is able to balance projects with day-to-day duties, ensuring participation from other members of the department as needed. - Is able to establish priorities and timelines to effectively manage workload. - Is able to multi-task well. - Deals with people in an honest and forthright manner representing information and data accurately. We captured all. - Why Choose Us? paragraph: we used as Benefits prose. Let's verify we captured all sentences: Original Why Choose Us?: "Bring the miracles of science to life alongside a supportive, future-focused team. Discover

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