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Ascendis Pharma

Biopharmaceutical company developing long-acting prodrugs

Director, Head of Global Labeling

Regulatory & Quality (Life Sciences)Confirmed live in the last 24 hours
Full-time$220k - $240k

About the Job

Requirements

  • Hold a relevant academic bachelor's degree from an accredited university.
  • Be proficient in English at a professional level.
  • Have 15 or more years of pharmaceutical industry experience, including at least 10 years in global regulatory affairs, extensive experience in global labeling strategy and operations, and at least 5 years of people leadership.
  • Have deep expertise in global labeling and regulatory requirements, including product labeling strategy, risk minimization, and regulatory compliance across global markets, with demonstrated experience establishing, leading, and continuously evolving a Global Labeling function and capability.
  • Have demonstrated success leading teams and influencing stakeholders in complex, matrixed, and cross-cultural environments.
  • Have strong strategic, communication, and organizational skills, with the ability to drive decisions, build effective relationships, and communicate complex scientific and regulatory concepts to diverse audiences.
  • Have strong digital and systems acumen and experience using regulatory information management and labeling systems.
  • Have a passion for advancing innovative therapies that address unmet medical needs for patients with rare endocrine diseases.
  • Be comfortable balancing strategic thinking with hands-on execution.
  • Have demonstrated ability to navigate uncertainty and adapt quickly to changing priorities in a global matrix organization.
  • Have a proven track record delivering results in dynamic, fast-paced settings where clarity evolves over time.
  • Be able to travel domestically and internationally up to 15% of the time.

Responsibilities

  • Lead the Global Labeling function and oversee the worldwide labeling portfolio for Ascendis endocrinology products.
  • Build and develop a collaborative global labeling team and operating model that delivers scientifically sound, regulatory-compliant core and local labeling while supporting portfolio growth.
  • Define and drive global labeling operations that support business objectives, optimize product benefit-risk communication, and meet regulatory and clinical requirements.
  • Provide strategic and operational labeling leadership and expert guidance to governance bodies, cross-functional stakeholders, local affiliates, and external partners.
  • Own and continuously improve labeling processes and governance, including leadership of the Global Labeling Committee and oversight of core labeling documents.
  • Ensure timely and compliant implementation of labeling changes globally.
  • Lead labeling-related audits, inspections, and governance activities, and represent Global Labeling on cross-functional review boards as needed.

Desired Qualifications

  • Experience with Veeva Vault.

About the Company

Ascendis Pharma

Biopharmaceutical company developing long-acting prodrugs

Ascendis Pharma uses its TransCon technology to create long-acting prodrugs for rare endocrine diseases, with expansions into oncology and ophthalmology. The platform temporarily attaches an unmodified drug to an inert carrier and releases the active drug in a predictable, sustained way after injection, reducing how often patients must dosing. It differentiates itself through a proprietary delivery system and a track record that includes marketed therapies like SKYTROFA for pediatric growth hormone deficiency and YORVIPATH for hypoparathyroidism, along with collaborations such as a Novo Nordisk deal. The company aims to improve patient outcomes by enabling easier, less frequent dosing while expanding its pipeline across rare endocrine diseases, cancer, and eye diseases.

Company size
1,001-5,000
Company stage
IPO
Headquarters
Gentofte Municipality, Denmark
Founded
2007

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