Senior Manager, RA TA Group, Regulatory Affairs(Oncology)

AbbVie's mission is to discover and deliver innovative medicines and solutions that solve serious health issues today and address the medical challenges of tomorrow. We strive to have a remarkable impact on people's lives across several key therapeutic areas – immunology, oncology, neuroscience, and eye care – and products and services in our Allergan Aesthetics portfolio. For more information about AbbVie, please visit us at www.abbvie.com. Follow @abbvie on X, Facebook, Instagram, YouTube, LinkedIn and Tik Tok.

Summary of Job Description:

The Senior Manager, Regulatory Affairs (RA) Therapeutic Area (TA) Group, Regulatory Affairs Japan, is responsible for leading a team of RA TA professionals within the assigned therapeutic area. This role ensures effective workflow, optimal productivity, professional development, and delivery of high-quality regulatory outputs in a timely manner. The Senior Manager develops and implements group strategies aligned with organizational objectives, provides leadership, mentors staff, drives operational excellence in both regulatory and therapeutic domains, and actively manages development projects as needed.

Major Responsibilities:

• Lead and manage the RA TA team by setting clear objectives and performance expectations.
• Oversee recruitment, onboarding, and ongoing training and development for all team members.
• Allocate projects and responsibilities based on regulatory and therapeutic area expertise, monitor progress, support team members, and ensure timely achievement of deliverables.
• Mentor and coach team members to support their professional and career growth.
• Direct involvement in development projects and life-cycle management activities, including Package Insert maintenance. Lead and implement local regulatory strategies as appropriate.
• Foster a collaborative and high-performing organizational culture within the RA TA group and with cross-functional teams.
• Liaise with key internal and external stakeholders (e.g., PMDA, MHLW, global teams) for cross-functional initiatives, including regulatory submissions and therapeutic projects.
• Identify, address, and resolve strategic and operational challenges impacting regulatory and therapeutic area activities.
• Contribute to regulatory policy intelligence and actively monitor relevant regulatory changes and developments.
• Ensure compliance with company policies and all applicable health authority regulations.

Essential Skills & Abilities:

• Leadership & Team Management: Demonstrated experience in leading, motivating, and developing diverse and cross-functional teams.
• Organizational Skills: Strong ability to prioritize tasks, coordinate multiple projects, and maintain high standards of quality and accuracy.
• Communication: Excellent verbal and written communication skills in Japanese and business level in English, with proven ability to collaborate cross-functionally and manage diverse stakeholders.
• Problem-Solving: Proactive, analytical, and solution-oriented mindset to identify and resolve challenges efficiently.
• Project Management: Proficiency in planning, executing, and monitoring projects to ensure delivery within scope and timelines.
• Compliance Orientation: Exceptional attention to detail with a robust understanding of regulatory frameworks and industry requirements.

Education / Experience Required:

• Bachelor’s or Master’s degree in a relevant field (e.g., Life Sciences, Regulatory Affairs, Public Health, Clinical Development, Engineering).
• Extensive experience managing teams and/or projects, preferably in Regulatory Affairs and within pharmaceutical or related industries.
• In-depth knowledge and hands-on experience in regulatory affairs, including regulatory strategy development and product lifecycle management.

アッヴィは、機会均等を重視する雇用主であり、誠実な企業活動、革新の推進、人々の生活への貢献、そして地域社会への貢献に努めています。雇用機会均等に向けて、障がいを持つ方々も積極的に支援しています。