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open role · workday:amgen

Japan Development Lead, Development TA (General Medicine)

$AMGNTokyo· posted Jul 22, 2026
ClinicalLead

Career Category Clinical Job Description Purposes of the job are,

• Accountable for leading the development and implementation of the Japan Clinical Development Plan (JCDP) which is a part of Japan Evidence Generation Plan (JEGP), incorporating local current medical/clinical insights into specific molecules in accordance with global development strategy (regardless of JPST Lead assignment)

• Expected to support other functional members in proceeding with all clinical activities/deliverables as planned

• Provide medical/clinical expertise to advance clinical development in Japan

• Assigned with a dual role for Japan Product Strategy Team (JPST) Lead, accountable for leading cross functional team discussions to develop the Japan Product Strategy (JPS) and the JEGP

Responsibilities include,

• Obtain global CDP for JPST members to adapt them into JCDP; ensure that the JCDP are based on multifaceted considerations aiming to maximize values for patients and Amgen

• Provide local medical/clinical input on treatment paradigms, guidelines, unmet needs to the global team in the CDP and study design

• Partner with Regulatory Affairs and Safety/ Value & Access (V&A) to define and maintain the product benefit/risk profile and facilitate local registration and reimbursement by providing medical/scientific leadership and input into key regulatory/safety deliverables, such as CTD, Regulatory responses, etc.

• Partner with Local Development Operations (including project specific cluster team) to provide strategic oversight and execution of clinical trials

• Support Local Development Operations and Local Medical Affairs in clinical study activity (e.g., a speaker at investigator meetings, regulatory inspection, supplemental local training at LST, and co-visit to clinical sites) following GDO-medical collaboration playbook for Japan

• As JPST Lead, lead the development of JPS and associated JEGP in aligned with Global Product Strategy (GPS)/ Global Brand Plan (GBP), and obtain endorsement from Japan Portfolio Review Committee (JPRC) following JPST playbook

• As JPST Lead, support the Local Medical Affairs, Marketing, and V&A in capturing and translating local/regional data gaps into actionable JEGPs, in alignment with GPS/GBP and EGP

• Encourage active and efficient work styles in accordance with the Team Charter and build an environment where each member can utilize their full potential

• Delegate/coach/support JDMs and develop their talent if applicable

• Proactively share lessons & learned and know-how from their project activities and contribute to organizational Kaizen

Qualifications Basic Qualifications

• 5 or more years of clinical development experience in the biopharmaceutical industry, and experience with clinical project lead or proven industry collaboration in academia

• Proven ability to lead multiple projects/indications and produce high-quality results

• Medical degree, PhD, and/or equivalent experiences of Master’s degree

• Fluency in English, both oral and written communications

• Business Japanese skill, both oral and written communications

Preferred Qualifications

• Experience to manage product life cycle management in collaboration across functions as a lead and/or representative from Clinical Development

• Experience to manage early phase of clinical trial

• Experience with NDA filing

Knowledge/ Experience

• Understanding of Japanese regulatory agency organization, guidelines, and practices and ability to negotiate with these groups

• Understanding of new drug product lifecycle and commercialization process with understanding of other functions; including but not limited to Clinical Operations, Commercial, Regulatory, and Medical Affairs, Value Access and Policy

• In-depth understanding of and proven success in how to conceptualize, design, and conduct complex, global clinical trials

• Medical knowledge in the relevant therapeutic area

• Sound scientific and clinical judgment

• Experience in leading Clinical Development and NDA filing

• Experience with clinical study management and conduct

• Knowledge of GCP, PMDA regulations, guidelines and compliance

Competencies

• Demonstrates Amgen Values and Leadership Attributes

• Demonstrates strategic mindset to enable challenging JEGP/JCDP for patients in Japan

• Demonstrates robust ability to build effective cross functional teams through collaboration

• Instills trust by following through on commitment and showing consistency between words and actions

• Be resilient in cross functional collaborations

• Anticipate the impact of emerging technologies and makes adjustments, in particular, for the strategic clinical planning

.

requirements

Basic Qualifications • 5 or more years of clinical development experience in the biopharmaceutical industry, and experience with clinical project lead or proven industry collaboration in academia • Proven ability to lead multiple projects/indications and produce high-quality results • Medical degree, PhD, and/or equivalent experiences of Master’s degree • Fluency in English, both oral and written communications • Business Japanese skill, both oral and written communications Preferred Qualifications • Experience to manage product life cycle management in collaboration across functions as a lead and/or representative from Clinical Development • Experience to manage early phase of clinical trial • Experience with NDA filing Knowledge/ Experience • Understanding of Japanese regulatory agency organization, guidelines, and practices and ability to negotiate with these groups • Understanding of new drug product lifecycle and commercialization process with understanding of other functions; including but not limited to Clinical Operations, Commercial, Regulatory, and Medical Affairs, Value Access and Policy • In-depth understanding of and proven success in how to conceptualize, design, and conduct complex, global clinical trials • Medical knowledge in the relevant therapeutic area • Sound scientific and clinical judgment • Experience in leading Clinical Development and NDA filing • Experience with clinical study management and conduct • Knowledge of GCP, PMDA regulations, guidelines and compliance Competencies • Demonstrates Amgen Values and Leadership Attributes • Demonstrates strategic mindset to enable challenging JEGP/JCDP for patients in Japan • Demonstrates robust ability to build effective cross functional teams through collaboration • Instills trust by following through on commitment and showing consistency between words and actions • Be resilient in cross functional collaborations • Anticipate the impact of emerging technologies and makes adjustments, in particular, for the strategic clinical planning .

skills Bork detected

GCPBLA / NDA FilingPMDA (Japan)Medical Affairs
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