* Manage timely product approvals for target indications in Japan
* Align with global strategies and Japanese healthcare requirements
* Collaborate across departments for regulatory compliance
* Develop and update Japanese clinical development plans
* Handle submissions and registrations
* Manage projects within Oncology therapeutic area
Client Details
* European headquartered pharmaceutical company and global leader developing groundbreaking therapies within Oncology, Immunology and Neurology
* With a global work force of over 50,000 employees, our client offers a culture that emphasizes empowerment, autonomy, inclusivity and innovation
Description
* This role involves managing the approval process for Oncology Assets, ensuring alignment with Japanese healthcare regulations and needs.
* Responsibilities include developing and updating clinical development plans, handling submissions and registrations, managing project timelines and quality, supporting management decisions, providing safety assessments, facilitating pricing negotiations, and transferring knowledge to relevant teams, including medical affairs and market access.
* Additionally, building and maintaining networks with external experts in Japan is crucial for the role.
Profile
* Licensed MD
* Native level Japanese
* Business level English
* Clinical practice and basic research in oncology/cancer preferred
Job Offer
* Have a wide impact on patients across Japan and further afield
* Meaningful position in a major global company
* Stable career path, overseas experience opportunities
* Expand medical expertise beyond clinical practise to medical affairs, clinical development and pharmacovigilance
Page Group Japan is acting as an Employment Agency in relation to this vacancy.

Oncology - Clinical Program Lead

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