Posted:
3/5/2025, 4:00:00 PM
Location(s):
Chiyoda City, Tokyo, Japan ⋅ Tokyo, Japan
Experience Level(s):
Mid Level ⋅ Senior
Field(s):
Business & Strategy
Job Description
新薬開発プロジェクトにおけるプロジェクトマネジメント業務 – プロジェクトマネジメントのスキルや専門知識、一般的ビジネススキル、および疾患領域特異的な知識や経験を基に、部門横断的および戦略的視点からプロジェクトを推進する。
・プロジェクトスコープの特定と開発戦略の立案を推進する。
・開発戦略の実行状況やタイムライン等の進捗管理を行う。
・リスクマネジメント、ステークホルダーマネジメントを遂行する。
・ガバナンスとプロジェクトの接点となり、開発戦略の意思決定を推進する。
・US本社プロジェクトマネージャーやチームメンバーと協働し、世界同時開発を推進する。
・他社との協働にあたり、アライアンスマネジメントを遂行する
・特許等様々な観点から、製品の価値最大化に貢献する。
【必要なスキル・経験】
・5年以上の製薬会社での勤務経験
・3年以上のプロジェクトマネジメント経験
・ビジネスレベルでの英語力(TOEIC 800点以上)
・日本語:ネイティブまたは流暢レベル
【尚可要件】
PMP (Project Management Professional) 資格
※ Grade:P3 (Sr. Specialist)での募集ですが、ご経歴によりP2 (Specialist) やP4 (Associate Director)で採用する場合がございます。
Current Employees apply HERE
Current Contingent Workers apply HERE
Secondary Language(s) Job Description:
Provide Japan Development Team with project and alliance management skill and knowledge with drug/vaccine development expertise and business acumen, in order to deliver JNDA filing, approval, and clinical studies milestones successfully in Japan.
Facilitate development strategy planning and execution of new drug development in Japan in collaboration with key stakeholders
Facilitate science based business decision-making at all level collaborating with governance committees
Share accountability with the Japan Project Lead for team effectiveness and taking accountability for team dynamics
Work very closely with global project managers in US HQ in order to achieve simultaneous development, filing and approval in Japan
Provide PM service from the perspective of timeline, cost/resource, risk, stakeholder and communication management
Provide AM service in collaborating with external partners
Contribute to the maximization of product value from patent/IP perspective
【Requirement】
More than 5 years experience in pharmaceutical industry, with greater than 3 years experience in Project Management.
English : Business levle (TOEIC >800)
Japanese: Fluent
【Preferred】
Certified Project Management Professional (PMP)
※ Grade: We are recruiting for P3 (Sr. Specialist), but depending on your career history, we may hire you as P2 (Specialist) or P4 (Associate Director).
Search Firm Representatives Please Read Carefully
Merck & Co., Inc., Rahway, NJ, USA, also known as Merck Sharp & Dohme LLC, Rahway, NJ, USA, does not accept unsolicited assistance from search firms for employment opportunities. All CVs / resumes submitted by search firms to any employee at our company without a valid written search agreement in place for this position will be deemed the sole property of our company. No fee will be paid in the event a candidate is hired by our company as a result of an agency referral where no pre-existing agreement is in place. Where agency agreements are in place, introductions are position specific. Please, no phone calls or emails.
Employee Status:
RegularRelocation:
VISA Sponsorship:
Travel Requirements:
Flexible Work Arrangements:
HybridShift:
Valid Driving License:
Hazardous Material(s):
Job Posting End Date:
08/31/2025*A job posting is effective until 11:59:59PM on the day BEFORE the listed job posting end date. Please ensure you apply to a job posting no later than the day BEFORE the job posting end date.
Website: https://www.merck.com/
Headquarter Location: Rahway, New Jersey, United States
Employee Count: 10001+
Year Founded: 1891
IPO Status: Public
Last Funding Type: Post-IPO Equity
Industries: Biotechnology ⋅ Health Care ⋅ Medical ⋅ Pharmaceutical