Tokyo, Japan · Remote OK
Company Description PSI is a leading Contract Research Organization (CRO) with over 25 years of experience in the pharmaceutical industry. Originating from Switzerland, PSI is a privately owned, full-service CRO with a g…
Skills: Clinical Trial Submissions, PMDA Regulations, Regulatory Dossier Preparation, English Proficiency, Japanese Proficiency
Tokyo, Japan · On-site
Company Description PSI is a leading Contract Research Organization (CRO) with over 25 years of experience in the pharmaceutical industry. Originating from Switzerland, PSI is a privately owned, full-service CRO with a g…
Skills: Project Management, Clinical Operations, Site Monitoring, KPI Management, Budget Negotiation
Tokyo, Japan · On-site
Company Description PSI is a leading Contract Research Organization (CRO) with 30 years of experience in the pharmaceutical industry. Originated in Switzerland, PSI is a privately owned, full-service CRO with a global re…
Skills: Medical Monitoring, Clinical Research, Pharmacovigilance, Clinical Development Planning, Regulatory Compliance
Tokyo, Japan · Hybrid
Site Contracting - Tokyo Osaka - Office Hybrid Home ICON is a global healthcare intelligence and clinical research organisation united by a mission to bring new medicines and treatments to patients faster. As a values-dr…
Skills: Contract Management, Contract Negotiation, Regulatory Compliance, Risk Analysis, Contract Drafting
Tokyo, Japan · Hybrid
Job Summary: 特定のプロジェクトチームの日本の薬事担当者として、薬事戦略の策定及び実施に積極的に貢献し、必要に応じて関連する規制当局と交渉を行う役割を担う。 日本のライフサイクルマネジメントを含め、新薬の承認申請資料の作成プロセスを管理する。 Job Duties: 規制に関する十分な知識に基づき、開発の全段階（第I相以前から市販まで）において担当するプロジェクトやプログラムの薬事戦略の策定と実施に積極的に貢献する責任を負う…
Skills: Regulatory Strategy, Regulatory Affairs, Lifecycle Management, Regulatory Negotiation, Submission Management
Tokyo, Japan · On-site
Clinical Pathway Capability Specialist Location: Tokyo Department: Sales Job type: Full Time Join us and make a difference when it matters most! At Mundipharma, we are proud of the work we do to bring innovative treatmen…
Skills: Capability Development, KAM Coaching, Instructional Design, Account Planning, Omnichannel Strategy
Tokyo, Japan · On-site
This is what you will do: 担当地区における医療関係者とAlexionの主要窓口として、疾患及び製品の認知度を向上させ、患者様の為に診療環境の整備に努める。 医療関係者との良好な関係を築き、診療におけるニーズを特定・整理し、担当製品関連の紹介・提案を行う。 また、担当地区の責任者としてエリアを管理し、潜在的な顧客や市場開発の可能性を見つけることにも従事する。 You will be responsible for…
Skills: Territory Management, Market Analysis, Rare Disease Knowledge, Medical Representative Skills, Stakeholder Collaboration
Tokyo, Japan · Hybrid
Payment Specialist - Tokyo Osaka - Office Hybrid Home ICON is a global healthcare intelligence and clinical research organisation united by a mission to bring new medicines and treatments to patients faster. As a values-…
Skills: Data Analysis, Financial Reporting, Tableau, Power BI, Advanced Excel
Tokyo, Japan · Hybrid
MENTAL HEALTH ADVISOR The Mental Health Advisor (MHA) provides culturally-informed counseling/psychotherapy, education, support, coaching, and case management services for university students through our Counseling & Psy…
Skills: Psychotherapy, Counseling, Case Management, Crisis Stabilization, Intercultural Communication
Tokyo, Japan · Hybrid
At Gilead, we’re creating a healthier world for all people. For more than 35 years, we’ve tackled diseases such as HIV, viral hepatitis, COVID-19 and cancer – working relentlessly to develop therapies that help improve l…
Skills: Strategic Thinking, Medical Affairs, People Management, Clinical Science, Evidence Generation
Tokyo, Japan · Remote OK
At Gilead, we’re creating a healthier world for all people. For more than 35 years, we’ve tackled diseases such as HIV, viral hepatitis, COVID-19 and cancer – working relentlessly to develop therapies that help improve l…
Skills: Pharmaceutical Sales, Negotiation, Influencing, Market Analysis, Territory Management
Tokyo, Japan · Hybrid
Position Summary You will lead health technology assessment (HTA) and evidence synthesis activities to support access and reimbursement in Japan. You will work with cross-functional colleagues in market access, clinical …
Skills: Evidence Synthesis, Health Technology Assessment, Systematic Literature Reviews, Meta-analysis, Health Economics
Tokyo, Japan · Hybrid
$300k/mo
At Roche you can show up as yourself, embraced for the unique qualities you bring. Our culture encourages personal expression, open dialogue, and genuine connections, where you are valued, accepted and respected for who …
Skills: Consultative Selling, New Business Development, Solution Selling, Relationship Management, ROI Analysis
Tokyo, Japan · Remote OK
At Gilead, we’re creating a healthier world for all people. For more than 35 years, we’ve tackled diseases such as HIV, viral hepatitis, COVID-19 and cancer – working relentlessly to develop therapies that help improve l…
Skills: Pharmaceutical Sales, Negotiation, Influencing, Market Analysis, Territory Management
Tokyo, Japan · Hybrid
$5500k–$7500k/yr
About ZEISS ZEISSグループは、創業者のカール ツァイスが1846年にドイツ東部の都市、イエナに開設した精密機器および光学部品の工房から急成長を遂げました。日本では1911年にカールツァイス株式会社が設立され、約400人の従業員が5つの事業所で販売とサービスを提供しています。ZEISS日本は半導体、自動車、機械工学、生物医学研究、医療技術のパートナーであり、眼鏡レンズやカメラレンズ、双眼鏡の大手メーカーでもあります。 職務…
Skills: Medical Device Sales, Proposal-based Selling, Project Management, CRM Software, Stakeholder Communication
Tokyo, Japan · Remote OK
At Gilead, we’re creating a healthier world for all people. For more than 35 years, we’ve tackled diseases such as HIV, viral hepatitis, COVID-19 and cancer – working relentlessly to develop therapies that help improve l…
Skills: Pharmaceutical Sales, Negotiation, Influencing, Market Analysis, Territory Management
Tokyo, Japan · Remote OK
At Gilead, we’re creating a healthier world for all people. For more than 35 years, we’ve tackled diseases such as HIV, viral hepatitis, COVID-19 and cancer – working relentlessly to develop therapies that help improve l…
Skills: Pharmaceutical Sales, Negotiation, Influencing, Market Analysis, Territory Management
Tokyo, Japan · Remote OK
At Gilead, we’re creating a healthier world for all people. For more than 35 years, we’ve tackled diseases such as HIV, viral hepatitis, COVID-19 and cancer – working relentlessly to develop therapies that help improve l…
Skills: Pharmaceutical Sales, Negotiation, Influencing, Market Analysis, Territory Management
Tokyo, Japan · On-site
About the Role Join our Digital & AI Transformation initiatives under Edwards Japan Quality team (Waku Waku DX Japan) working on real-world, Digital tools, and AI systems. This internship is designed not only as a learni…
Skills: Software Engineering, Object-Oriented Programming, Python, AI/ML, Data Engineering
Tokyo, Japan · On-site
Company Description PSI is a leading Contract Research Organization (CRO) with 30 years of experience in the pharmaceutical industry. Originated in Switzerland, PSI is a privately owned, full-service CRO with a global re…
Skills: Medical Monitoring, Clinical Research, Pharmacovigilance, Clinical Development Planning, Protocol Development
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The Regulatory Officer prepares clinical trial dossiers for regulatory authorities and manages communications with stakeholders, sponsors, and vendors. They are also responsible for tracking legislative changes in Japan and delivering regulatory training to project teams.
Candidates must hold a university degree in Life Sciences, Medicine, Pharmacy, or a related field. Proficiency in both English and Japanese, along with experience in clinical trial submissions to the PMDA, is required.
PSI is a leading Contract Research Organization (CRO) with over 25 years of experience in the pharmaceutical industry. Originating from Switzerland, PSI is a privately owned, full-service CRO with a global reach, supporting clinical trials across multiple countries and continents. Our reputation for being highly selective about the projects we undertake highlights our commitment to delivering high-quality, timely services across a broad spectrum of therapeutic indications.
In an industry where cost-cutting and layoffs are common, PSI stands out as a stable and secure workplace. Our dedication to stability is evident in our exceptionally high repeat and referral business rate and minimal staff turnover. Many of our colleagues have been with us for over 15 years, contributing to our long-standing traditions and history. Our expansion into Japan continues this legacy, and we seek team members who will grow with us for the long term.
At PSI, we foster an environment where a diverse range of colleagues feel welcomed and valued. Our inclusive culture is a cornerstone of our success, enabling us to attract and retain top talent globally.
We are not just about conducting clinical trials; we are about building a community where every team member has the opportunity to thrive and contribute to groundbreaking advancements in the pharmaceutical industry.
As a Regulatory Officer, you will work closely with our global team of experts to prepare clinical trial dossiers for regulatory authorities, deliver regulatory training to project teams, and communicate with stakeholders on regulatory-related matters. Join PSI and help drive innovation and excellence in advancing healthcare solutions.
Location: Tokyo preferred (Osaka or remote within Japan is negotiable)
Level: Open from Junior to Mid level candidates
PSI is privately owned by the very people who founded the company more than 25 years ago, and they’re still working here today. As a result, we have grown organically around the globe and have kept our company fully independent, giving us significant advantages and freedoms.
As a part of the PSI team, you will have a fair degree of ownership and autonomy to make nuanced country-and department-specific adjustments while nurturing the global PSI culture that unites us across six continents.
You will receive continuous support from your global peers and join a fast-paced, innovative, and results-oriented working environment with lean communication lines. We pride ourselves on being approachable, receptive to new ideas, and open to feedback.
PSI is proud to invest in our people, from entry-level team members to senior leaders, helping you identify and hone your unique strengths at every step of your career. From on-the-job learning experiences to formal development programs, our professionals have a variety of opportunities to continue to grow throughout their career.
PSI is an inclusive and equal opportunity employer and is committed to attracting and retaining a diverse workforce that reflects the community we serve.
PSI is a leading full-service global Contract Research Organization whose key strength is predictable patient enrollment across multiple therapeutic areas. PSI is known in the industry as a CRO focused on ‘on-time project delivery’. This is achieved through investing substantial effort and MD resources into performing quality feasibility assessments that provide an accurate predictor of study timelines. PSI’s global reach allows us to run clinical trials across multiple continents, in 50+ countries around the world. PSI’s reputation is that of a 'no-nonsense' CRO focused on timely patient enrollment and project delivery. An exceptionally high repeat and referral business rates alongside low staff turnover are indicative of our commitment to be the best CRO in the world as measured by our clients and our employees. http://www.psi-cro.com
Offices: Baarerstrasse 113a, Zug, 6300, CH
There are currently 134 open healthcare positions in Tokyo, Japan listed on Clera. New openings are added daily as companies post roles.
Companies currently hiring include PSI CRO, Amgen, AstraZeneca, GSK, Gilead Sciences, among others. Browse the listings above to see every active employer.
Yes — 70 of the 134 open healthcare positions offer remote or hybrid work (16 remote, 54 hybrid).
Each listing links directly to the employer's application page. Apply early — fresh listings get the most recruiter attention in the first two weeks.
