19 часов назад
Medical Affairs Director, Medical Operations (Biopharmaceuticals)
Мэтч & Сопровод
Для мэтча с этой вакансией нужен Plus
Описание вакансии
Текст:
TL;DR
Medical Affairs Director, Medical Operations (Biopharmaceuticals): Leading global and local medical operations, governance, resource management, and process improvement for a biopharmaceutical organization with an accent on Medical Affairs transformation, regulatory compliance, and integrated planning. Focus on designing operational standards, solving organizational inefficiencies, managing budgets and metrics, and building high-performing teams across Japanese and global stakeholders.
Location: Japan; hybrid work environment in the Tokyo office. Domestic and international travel of at least 10% is required.
Company
is a global biopharmaceutical company focused on transforming the lives of patients with serious and rare diseases.
What you will do
- Develop and implement standards, tools, templates, governance procedures, and operational methods for Medical Affairs.
- Manage budgets, resources, systems, timelines, milestones, and external vendors for medical activities.
- Identify business challenges and inefficiencies, conduct root cause analysis, and lead organizational and process improvement initiatives.
- Coordinate global harmonization and local adaptation with Medical Affairs stakeholders and support integrated Medical Action Plans.
- Develop communication plans, metrics, and reporting to measure and optimize the impact of Medical Affairs activities.
- Lead Medical Affairs transformation, regulatory alignment, cross-functional collaboration, and the development of high-performing teams.
Requirements
- Bachelor’s degree or higher; an MBA is preferred.
- 15+ years of relevant professional or industry experience, including 10+ years of hands-on Medical Affairs experience.
- Strong program management, strategic thinking, change management, problem-solving, communication, and listening skills.
- Deep knowledge of Medical Affairs responsibilities and the pharmaceutical industry regulatory environment.
- Ability to lead through influence, manage vendors, work independently, anticipate risks, and ensure compliance across departments.
- High communication skills in Japanese and English are required; the role is based in Japan and uses a hybrid work environment.
Culture & Benefits
- Flexible working hours and vacation programs supporting work-life balance.
- Retirement benefits, equity compensation, and access to an employee stock purchase plan.
- Internal and external training, LinkedIn Learning, and role-specific professional development.
- AI-powered learning tools and digital assistant access to internal resources.
- Global recognition programs, employee resource groups, modern collaboration technology, and IT support.
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