Associate Director

The Regulatory Affairs (RA) Associate Director, Labeling will be responsible for labeling activities across programs and stages of development, with specific responsibility for the United States and the Americas and supporting global needs as required.

The RA Associate Director, Labeling will be overall responsible for ensuring compliance with US regulatory requirements for labeling, and for coordinating internal labelling activities and processes for regulatory submissions and product maintenance. The Associate Director prioritizes their own work to meet agreed timelines and works both independently and in a team environment. Global coordination is also required and work with external partners may be required.

Key responsibilities:

Drive process for development and management of US & Americas labelling content for initial and updated labels, including working with the Global Regulatory Lead for developing key messaging and strategy

Provide labeling advice and expertise on Company Core Data Sheet (CCDS), USPI and Canadian Monograph content, and collaborate with other market leads to develop local labeling in line with global strategies and local regulations

Coordinate US labeling activities for regulatory submissions, product maintenance and safety variations, including developing timelines, involving relevant SMEs, and handling reviews

Understand and interpret regulatory requirements for labelling to meet applicable regulations

Perform global label competitive intelligence, and make recommendations for actions

Plan, support and advise in liaison and negotiation with FDA and other agencies as needed for labelling content

Ensure and maintain tracking and archiving of approved labels

Develop project timelines and manage labeling projects from initiation to completion

Contribute to development of key labeling processes and infrastructure

Work closely with global labeling managers to ensure consistency and alignment

Requirements

BS/BA or equivalent degree in a Scientific Discipline, advanced degree desirable

Regulatory experience of at least 8 years, and at least 3 years direct experience with labeling in the US

Solid knowledge of regulatory labelling requirements in the US, have an understanding of current global and regional trends and ability to assess the impact of these requirements

Experience working in international teams

Excellent collaboration and communication skills

Preference for creative thinking and solution development

Ability to interact cross-functionally with members of commercial, legal, safety, medical, and others

Proficient in document editing including Microsoft office applications (Word, PowerPoint, Excel)

Experience in systems (e.g. document management systems, labeling systems, etc.

Recognize when to provide labeling guidance to product strategy teams, product review teams, HA response teams, labeling stakeholders, junior team members, or others as needed

Strong understanding of the purpose of the Target Product Label and CCDS and the associated implications on labeling globally, downstream processes, and compliance needs

Participates with influence in or leads departmental and cross-functional taskforces and initiatives

Interpret labeling regulations and guidance

Responds to challenging situations in a calm and confident manner

Embraces change and quickly alters course in response to new challenges

Ability to travel up to 10% of the time domestically and internationally

Estimated compensation: $180-200K/year

A note to recruiters:

We do not allow external search party solicitation. Presentation of candidates without written permission from the Ascendis Pharma Inc Human Resources team (specifically from: Talent Acquisition Partner or Human Resources Director) is not allowed. If this occurs your ownership of these candidates will not be acknowledged.

Benefits

Medical insurance

Vision insurance

Dental insurance

401(k)

Paid maternity leave

Paid paternity leave

Commuter benefits

Disability insurance