Associate Director, Global Labeling Strategy Lead

Work Location:  Billerica, Massachusetts

Shift:

Department:  HC-RD-RPO TA Oncology / ImmunoOncology

Recruiter:  Sarah Ellis

This information is for internals only. Please do not share outside of the organization.

Your Role:

The Associate Director of Global Labeling / Labeling Product Lead (LPL) ensures globally harmonized product labeling in close collaboration with cross-functional labeling product teams by leading the creation and maintenance of Company Core Data Sheets (CCDS), regional labeling documents including US/EU product information (PIs), and global packaging text in compliance with regulatory standards. The LPL supports country regulatory affairs (CRA) in creating national product information (NPI) ensuring consistency with the CCDS or a reference label. The LPL is  the subject matter expert on labeling-related health authority queries and may also develop target product labeling content for development products.

Location: This is a hybrid, 3x/week in office position based in Billerica, MA

Key Accountabilities:

Create and maintain global CCDS in collaboration with product teams to serve as the basis for worldwide harmonized labeling. In some cases, maintain RSI to represent company position.

Manage the creation and maintenance, review and approval of US and EU PIs ensuring consistency with the CCDS.

Lead cross-functional labeling team, prepare for and present proposals to the Labeling Senior Management Board, and secure internal approval of labeling content.

Oversee and support implementation of CCDS content into local PIs.

Coordinate and respond to labeling inquiries from health authorities and participate in regulatory negotiations.

Lead the development of target product labeling content for development products, as needed.

Provide competitive labeling analyses and maintain up-to-date knowledge of local and regional labeling requirements.

Develop/contribute to labeling-related process documents and guidelines, propose company comments on regulatory initiatives, and drive cross-functional labeling initiatives.

Train product labeling teams on labeling processes, guide other labeling experts on life-cycle management, and cultivate relationships with regulatory professionals, associations, and authorities.

Minimum Qualifications

Bachelor’s degree in science or health-related discipline

5+ years of relevant pharmaceutical industry experience with 3+ years of relevant Regulatory Affairs Labeling experience

Deep knowledge and application of labeling requirements in the US/EU

Preferred Qualifications

Advanced degree (PhD, MD, MS, PharmD, MBA)

Advanced proficiency with MS Office (Word, Excel, PowerPoint, Project), SharePoint and regulatory systems (e.g., EDMS)

Meticulous in reviewing regulatory documents for accuracy, consistency, and compliance

Excellent written and oral communication skills

Knowledge and application of labeling requirements in global countries including Japan and China

Knowledge of global drug ‐ development and life ‐ cycle management regulations

Pay Range for this position: $134,200 - 202,200

The offer range represents the anticipated low and high end of the base pay compensation for this position. The actual compensation offered will be determined by factors such as location, level of experience, education, skills, and other job-related factors. Position may be eligible for sales or performance-based bonuses. Benefits offered by the Company include health insurance, paid time off (PTO), retirement contributions, and other prequisites. For more information click  here .

The Company is an Equal Employment Opportunity employer. No employee or applicant for employment will be discriminated against on the basis of race, color, religion, age, sex, sexual orientation, national origin, ancestry, disability, military or veteran status, genetic information, gender identity, transgender status, marital status, or any other classification protected by applicable federal, state, or local law.  This policy of Equal Employment Opportunity applies to all policies and programs relating to recruitment and hiring, promotion, compensation, benefits, discipline, termination, and all other terms and conditions of employment. Any applicant or employee who believes they have been discriminated against by the Company or anyone acting on behalf of the Company must report any concerns to their Human Resources Business Partner, Legal, or Compliance immediately. The Company will not retaliate against any individual because they made a good faith report of discrimination.