Instagram
youtube
Facebook

Director, Global Regulatory Lead, Gi & Inflammation

8+ years
$169,400.00 - $266,200.00
10 April 28, 2025
Job Description
Job Type: Full Time Education: PharmD/MD/PhD 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

Job Title: Director, Global Regulatory Lead, GI & Inflammation
Location: Boston, Massachusetts
Job Level: Senior
Travel: Minimal (if any)

Job ID: R0145516
Date Posted: 02/25/2025

Job Description:

Objective / Purpose:

  • Defines, develops, and leads global strategies to maximize regulatory success for complex and/or multiple projects.

  • Provides strategic and tactical advice to teams to achieve timely development and maintenance of programs, ensuring compliance with regulatory requirements.

  • Serves as a leader in both the department and within R&D, contributing to cross-functional initiatives and influencing the field.

  • Provides leadership and development for direct reports, including those serving as global regulatory leads.

Accountabilities:

  • Leads Global Regulatory Teams (GRTs) and applicable sub-working groups, such as the Label Working Group, ensuring global regulatory strategy execution.

  • Ensures global regulatory strategies are implemented and maintained in line with regulatory and business changes.

  • Communicates with key stakeholders to inform them of developments impacting regulatory success.

  • Proactively anticipates risks and develops solutions with team and management.

  • Responsible for US FDA submissions and approvals for assigned projects or overseeing direct reports.

  • Manages relationships with health authorities and FDA meetings.

  • Oversees vendor responsibility for regulatory activities and submissions.

  • Participates in departmental and cross-functional task forces.

  • Leads regulatory reviewer in due diligence for licensing opportunities.

  • Partners with global market access colleagues on regulatory/health agency/HTA bodies.

Education & Competencies:

  • Bachelor’s degree in scientific discipline (advanced degree preferred).

  • 8+ years in pharmaceutical industry with 6 years in regulatory experience (or 4+ years combined regulatory/related experience).

  • Experience in reviewing, authoring, or managing regulatory submissions.

  • Strong knowledge of FDA, EU, Canada, ROW, and post-marketing regulatory requirements.

  • Strong communication, negotiation, and problem-solving skills.

  • Ability to work effectively with global teams.

Compensation:

  • U.S. Base Salary Range: $169,400.00 - $266,200.00

  • Employees may be eligible for short-term/long-term incentives, benefits, and paid time off.

EEO Statement:

Takeda is committed to creating a diverse workforce and providing equal employment opportunities.