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Associate Director, Global Regulatory Affairs

7+ years
Not Disclosed
10 Oct. 23, 2024
Job Description
Job Type: Full Time Education: B.Sc./ M.Sc./ M.Pharm/ B.Pharm/ Life Sciences Skills: Causality Assessment, Clinical SAS Programming, Communication Skills, CPC Certified, GCP guidelines, ICD-10 CM Codes, CPT-Codes, HCPCS Codes, ICD-10 CM, CPT, HCPCS Coding, ICH guidelines, ICSR Case Processing, Interpersonal Skill, Labelling Assessment, MedDRA Coding, Medical Billing, Medical Coding, Medical Terminology, Narrative Writing, Research & Development, Technical Skill, Triage of ICSRs, WHO DD Coding

Associate Director, Global Regulatory Affairs

Company Overview
Global Regulatory Affairs (GRA) at Takeda develops and executes innovative regulatory strategies to deliver life-changing therapies to patients. GRA plays a strategic role in all stages of global product development across the Takeda Enterprise. We are committed to fostering a growth mindset and providing transformational opportunities for every team member.

Job ID: R0136180
Date Posted: 10/11/2024
Location: Boston, Massachusetts

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Job Description

Takeda Development Center Americas, Inc. is seeking an Associate Director, Global Regulatory Affairs in Cambridge, MA.

Key Responsibilities

  • Serve as the Global and US Regulatory Strategic Lead (GRL) for the immunology and inflammation therapeutic franchise on the global project team (GPT) for specific projects.

  • Provide global regulatory oversight and execute regulatory activities for late-stage development across multiple indications, device platforms, and cell line changes.

  • Manage interactions with health authorities, including preparation for meetings with the FDA (Type B, end of phase 2 meetings), EMA, BRDD (Canada), and PMDA (Japan).

  • Lead the development of global regulatory supplemental biologic application (sBLA) strategies and coordinate the global cross-functional submission working group.

  • Drive global submission strategy across various respiratory indications and collaborate with the global regulatory team to ensure successful pre-submission meetings and marketing application submissions.

Qualifications

  • Education: Master’s degree in Pharmacy, Biomedical Engineering, Regulatory Affairs, or a related field.

  • Experience: Minimum of 7 years of relevant experience in regulatory affairs.

  • Proven experience in global regulatory oversight, particularly in immunology and inflammation.

  • Strong background in preparing for and leading health authority interactions.

  • Ability to travel domestically and internationally, up to 20%.

Compensation

  • Salary Range: $212,400.00 - $290,400.00 per year.

To apply, please visit jobs.takeda.com and search for Req # R0136180.