武田薬品工業株式会社のAssociate Medical Director, Oncology Clinical Sciences, R&D, Osaka求人

武田薬品工業株式会社

職種
年収
エリア
大阪

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仕事内容

We are responsible for leading and driving the strategy for global clinical development, considering medical, scientific, regulatory, and commercial aspects for multiple pipeline compounds. Our mission involves influencing senior leadership's decision-making by setting strategic directions, designing, aligning, piloting, and establishing new development processes that require cross-functional collaboration within Takeda R&D. Success in this role directly impacts our corporate goals and Takeda's future commercial products. We lead multidisciplinary teams, such as the Global Clinical Lead (GCL), and require knowledge that extends beyond clinical and disease-area expertise to include broad areas of drug development.

Responsibilities include participating in and leading clinical development teams across the US, EU, and Japan, ensuring proactive identification of contingencies, potential risks, and strategies to address future challenges. We oversee the development team's strategy and deliverables, guiding the Development Strategy, Clinical Development Plan, and Clinical Protocols, while also recommending program scope and complexity. We ensure continual critical evaluation of development strategy to maintain competitive and state-of-the-art development plans.

Furthermore, we drive activities related to protocol development, study execution, and study interpretation, advising clinical scientists and ensuring successful project completion. We oversee medical monitoring activities in conjunction with Pharmacovigilance, assess safety information, and guide interactions with regulatory authorities and key opinion leaders. Leading R&D teams and participating in global cross-functional teams, we are accountable for staff hiring, mentoring, motivating, and retaining to support assigned activities. Our work requires superior communication, strategic, interpersonal, and negotiating skills, with an ability to lead complex, multi-regional matrix teams effectively.

募集要項

勤務地- Headquarters: Osaka/Tokyo
- Production Sites: Osaka/Yamaguchi/Narita
- Research Site: Kanagawa
給与- 昇給:年1回
- 賞与:年2回

給与の記載はありません。
勤務時間1. Headquarters (Osaka/ Tokyo) 9:00-17:30
2. Production Sites (Osaka/ Yamaguchi) 8:00-16:45
3. Production Site (Narita) 8:30-17:15
4. Research Site (Kanagawa) 9:00-17:45

フレックスタイム制も利用可能。
休暇制度Holidays: Saturdays, Sundays, National Holidays, May Day, Year-End Holidays etc. (approx. 123 days in a year).
Paid Leaves: Annual Paid Leave, Special Paid Leave, Sick Leave, Family Support Leave, Maternity Leave, Childcare Leave, Family Nursing Leave.
待遇・福利厚生- Allowances: Commutation, Housing, Overtime Work etc.
- Salary Increase: Annually
- Bonus Payment: Twice a year
- Working Hours: Headquarters (Osaka/ Tokyo) 9:00-17:30, Production Sites (Osaka/ Yamaguchi) 8:00-16:45, (Narita) 8:30-17:15, Research Site (Kanagawa) 9:00-17:45
- Holidays: Saturdays, Sundays, National Holidays, May Day, Year-End Holidays etc. (approx. 123 days in a year)
- Paid Leaves: Annual Paid Leave, Special Paid Leave, Sick Leave, Family Support Leave, Maternity Leave, Childcare Leave, Family Nursing Leave
- Flexible Work Styles: Flextime, Telework
- Benefits: Social Insurance, Retirement and Corporate Pension, Employee Stock Ownership Program, etc.
リモートワーク-
その他- **応募要件**: MD or internationally recognized equivalent plus 3 years of clinical research experience within the pharmaceutical industry, CRO health-related consulting company, or biomedical/clinical experience within academia (or a combination of afore mentioned). Previous experience successfully leading a clinical development team/matrix team with responsibility for studies. JNDA/NDA/MAA/Submission experience preferred.

- **望ましい経験**: Experience with and demonstrated ability to lead and manage highly trained medical, scientific and technical professionals preferred.

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