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Sobi

Develops therapies for rare diseases

Head of Global Regulatory Advertising and Promotion

Regulatory & Quality (Life Sciences)Confirmed live in the last 24 hours
Full-timeWaltham, MA, USA

About the Job

Requirements

  • A minimum bachelor's degree in a scientific discipline is required.
  • At least 15 years of experience in the pharmaceutical industry and at least 5 years as a regulatory Advertising and Promotion professional are required.
  • Expert knowledge of advertising and promotion regulations and FDA guidance documents, with technical experience in aspects of drug development and labeling, is required.
  • Advanced experience with promotional and medical review supporting product communications and working with FDA on advertising and promotion matters is required.
  • Advanced understanding of FDA promotional regulations, industry trends, the regulatory landscape, product and therapeutic knowledge, and evidentiary standards required to support product claims is required.
  • Ability to apply advanced regulatory experience and business knowledge to develop new ideas and best practices that support Sobi is required.
  • Ability to identify issues and convey facts, risk-mitigation strategies, and guidance, including the impact to Sobi without sufficient risk mitigation, is required.
  • Understanding of company objectives while executing regulatory strategies that deliver efficacious and FDA-compliant outcomes is required.
  • Ability to foresee vague or challenging situations and strategize to prevent or mitigate negative impact is required.
  • Ability to build agreement and acceptance, present a compelling case for ideas, negotiate persuasively, and address disagreements constructively is required.
  • Ability to plan, prioritize, and execute individual work, teamwork, and projects while balancing quality, cost, risk, and benefits is required.
  • Proficiency in using AI digital tools is required.

Responsibilities

  • Lead and direct post-marketing regulatory activities related to marketing Sobi products, including regulatory review and approval of U.S. promotional, corporate, and medical communications for assigned brands, submissions to FDA OPDP/APLB, and ownership of the Sobi Global Material review process.
  • Lead interactions with the FDA Office of Prescription Drug Promotion and function as a leader during review and escalation meetings to support compliance and evolution of the review process while meeting business needs.
  • Collaborate with cross-functional partners to provide regulatory advice and guidance throughout the product life cycle and ensure conformity with applicable laws, regulations, and Sobi policies.
  • Provide vision and strategy for the Ad & Promo team and lead team members reporting to the role.
  • Develop and lead departmental strategic initiatives.
  • Serve as a strategic partner to internal leadership on regulatory risk assessment and mitigation.
  • Oversee and direct the Ad & Promo team in assessing regulatory context and interpreting applicable guidance, regulations, and regulatory precedents.
  • Serve as the business owner of the Global Review Process.
  • Provide regulatory advice and guidance on advertising and promotion for global promotional and non-promotional materials.
  • Serve as an internal subject matter expert on FDA advertising and promotion issues, advise on regulatory concerns in draft promotional materials, and offer solutions to ensure FDA compliance.
  • Lead interactions with OPDP/APLB, including proactive engagement in support of business needs and responding to regulatory inquiries as needed.
  • Foster business partnerships with cross-functional stakeholders to support strategic business objectives.
  • Provide regulatory training as needed on applicable laws, regulations, and Sobi policies.
  • Serve as the regulatory reviewer on Review Committees.
  • Lead development of standard operating procedures and work instructions to drive compliance through streamlined workflows and efficient execution of relevant processes.

Desired Qualifications

  • An advanced scientific degree, such as a PhD, MD, or PharmD, or a Juris Doctor is preferred.
  • Experience in rare diseases, hematology, and/or oncology is a plus.

About the Company

Sobi

Develops therapies for rare diseases

Sobi specializes in developing and delivering therapies for rare diseases. It focuses on hematology, immunology, and specialty care, bringing medicines to patients who have limited treatment options. Their products are designed to treat rare conditions and are typically administered by prescription under medical supervision; the company collaborates with partners to advance research, develop, and commercialize these therapies. Sobi differentiates itself through its strong biotechnological foundation from its Biovitrum heritage and a track record of strategic collaborations with major pharmaceutical players like Sanofi and Apellis, which expand its research capabilities and reach. The company’s goal is to improve the lives of patients with rare diseases worldwide by creating and delivering effective treatments that address unmet medical needs.

Company size
1,001-5,000
Company stage
IPO
Headquarters
Solna kommun, Sweden
Founded
1988

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