# Senior Manager Clinical Pharmacology at UCB

UCB is hiring a Senior Manager Clinical Pharmacology in Tokyo, Japan. Level rates it Little AI ●○○○; you can [apply on UCB](https://jobsbylevel.com/go/f8bf154c-f3a0-4f7e-97dc-47759588bdc0?utm_medium=ai-agent).

AI Level 1, AI centrality 20 out of 100. Tokyo, Tokyo, Japan.

## Details

- Company: [UCB](https://jobsbylevel.com/companies/ucb)
- AI level: AI Level 1 (score 20 out of 100)
- Location: Tokyo, Tokyo, Japan
- Posted: November 6, 2026
- Apply: https://jobsbylevel.com/go/f8bf154c-f3a0-4f7e-97dc-47759588bdc0?utm_medium=ai-agent
- Free CV review for this job: https://jobsbylevel.com/cv-review?job=senior-manager-clinical-pharmacology-at-ucb-b36f21

## Prepare for this job

The job page lists 4 likely interview questions for this offer, with a CV checklist: https://jobsbylevel.com/jobs/senior-manager-clinical-pharmacology-at-ucb-b36f21

## Description

Make your mark for patients 患者さんのためにあなたの力を発揮してください JOB SUMMARY This is a regionally-focused, though globally-integrated, role which covers early through late phase development in SE Asia. The primary purposes of this position are: Contribute to assigned projects as Clinical Pharmacology specialist Propose exploratory phase clinical development strategy to minimize later stage development timelines in East Asia and to ensure simultaneous development in East Asia with Global development Ensure optimal Clinical Pharmacology support to all development programs up to submission for successful regional approvals Be responsible for Clinical Pharmacology part of IBs and CTDs, as well as regulatory correspondences and regulatory agency interactions Plan and conduct Clinical Pharmacology studies to allow comprehensive compounds’ characterization in Asians, to demonstrate ethnic insensitivity and substantiate CTD Understand and champion a model-based approach for drug development to achieve the above objectives. With a global development perspective, drive strategic planning to strengthen the expertise of clinical pharmacology Plan adequate allocation of human resource and number of studies, and control budget Expand coverage of clinical pharmacology for SE Asian development Establish the network with external specialists (PK and Clinical pharmacology field ) Establish the network with UCB Global counterparts. Where appropriate, drive strategies for novel (or non-standard) regulatory agency data expectations for regional drug approvals Responsible for clinical pharmacology activities, timelines and resources with adequate quality Ensure that processes, SOPs, and standardized training/tools exist to facilitate consistent, efficient and compliant clinical pharmacology deliverables Establish good relationship with Contract Research Organizations (CROs) for Clinical Pharmacology activities Mentor Clinical Pharmacologists to foster efficient collaboration with all necessary interfaces and to ensure the delivery of reliable and comprehensive deliverables in a timely fashion In concordance with respective global processes, lead to establish, as well as continually improve, regional standards of procedures, tools and technologies for clinical pharmacology Collaborate to provide input into global strategic/technical aspects Assist to planning and controlling functional budget. MAJOR ACCOUNTABILITIES Responsibility/co-responsibility for the Clinical Pharmacology program(s), pertaining to SE Asia development, for allocated projects including: Develop the Clinical Pharmacology part in Clinical Plan Plan and conduct Clinical Pharmacology study(ies) to assure global data bridging and East Asia’s participation into global P2 and/or P3 trials Representative of Clinical Pharmacology in Joint Clinical Study Team/Development teams Close collaboration with Research, Non-clinical and CS&S and other functions Provide Clinical Pharmacology expertise to assigned Clinical Study and Development teams Assess clinical data to evaluate ethnopharmacology considerations. Responsibility/co-responsibility for Clinical Pharmacology parts of main documents including Investigator’s Brochures, Protocols, Clinical Study Reports and all submission relevant documents Assessment of the scientific/medical quality of external Clinical Pharmacology Units in close collaboration with Global Exploratory Development and Outsourcing & Contracting Represents/co-represents Clinical Pharmacology for market approval submission to regulatory authorities, authority meetings and answers to all related authority questions Input to licensing projects on demand of Business Development or others as well as active scouting for potential relevant projects for in-licensing Cooperation with Commercial functions including publications, presentations, conference participation Responsibility for assigned Clinical Pharmacology trials including communication with the investigator review of the trial and

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