Last updated: 2025-05-22

43 Biopharmaceutical Leadership jobs in Tokyo.

Hiring now: Fsp Clinical Research Ass @ Parexel, Mgr Drug Safety @ Biogen, Medical Scientific Mgr @ Biomarin P, Pv Associate @ Ergomed, Lead Spec Regulatory Affa @ Stryker, Medical Affairs Mgr Oncol @ Pfizer, Regulatory Affairs Spec M @ Intuitive , Sr Mgr International Regu @ Biomarin, Cra 臨床開発モニター @ Iqvia, Multichannel Strategy Sr @ Veeva Syst.Explore more at at kaamvaam.com

🔥 Skills

Clinical Trials (6) project management (6) Clinical Research (5) pharmaceutical (5) clinical trials (4) pharmacovigilance (4) Regulatory Affairs (4) medical devices (4) regulatory submissions (4) biotechnology (4)

📍 Locations

Tokyo (43)

Parexel

Skills & Focus: Clinical Research Associate, CRA, monitoring duties, investigator sites, patient safety, oncology, clinical trials, biopharmaceuticals, global studies, CRO
About the Company: Parexel is a leading global biopharmaceutical services organization that provides a wide range of services to help clients bring innovative therapies to market.
Experience: 1 year or more in global studies, oncology experience

Biogen

Skills & Focus: Drug Safety, Pharmacovigilance, Regulations, Clinical Trials, Signal Management, Compliance, Quality Management System, Process Improvement, Vendor Management, NDA

Biomarin Pharmaceutical Inc.

Skills & Focus: observational research, Phase IIIb/IV studies, medical monitoring, post-marketing surveillance, clinical practice, Real World Data, Epidemiology, clinical study, scientific input, collaboration
Experience: 3+ years of clinical trial or post-marketing trial experience either at a study site or within the biopharmaceutical industry or within a Contract Research Organization.

Parexel

Skills & Focus: Clinical Research, Clinical Trials, Health Care, Project Management, Data Management, Regulatory Compliance, Patient Safety, Protocol Development, Statistical Analysis, Quality Assurance

Ergomed

Skills & Focus: pharmacovigilance, drug safety, clinical trials, data entry, reconciliation, report processing, post-marketing, GMP, pharmacovigilance activities, medical

Stryker

Skills & Focus: Regulatory Affairs, approval applications, medical devices, PMDA consultations, QMS compliance, certification, communication, project management, healthcare outcomes, medical insurance
About the Company: Stryker offers innovative products and services in MedSurg, Neurotechnology and Orthopaedics that help improve patient and healthcare outcomes. Alongside its c…
Experience: 3+ years of experience of medical device (Class I to IV) application approvals
Type: Full Time
Benefits: Health benefits include: Medical and prescription drug insurance, dental insurance, vision insurance, critical illness …

Pfizer

Skills & Focus: Medical Affairs, Oncology, Clinical Trials, Medical Strategy, Stakeholder Engagement, Scientific Exchange, Medical Education, Health Disparities, Real-World Evidence, Regulatory Compliance
About the Company: A leading pharmaceutical company dedicated to discovering, developing, and providing innovative medicines and vaccines.
Experience: Mid-Senior level
Type: Full-time
Benefits: Health insurance, retirement plans, professional development opportunities

Intuitive Surgical

Skills & Focus: regulatory affairs, NMPA, medical device, product registration, regulatory compliance, project management, team collaboration, regulatory submissions, clinical strategy, product lifecycle
About the Company: A pioneer and market leader in robotic-assisted surgery, committed to advancing minimally invasive care through innovative technology.
Experience: Minimum 3 years RA experience, 1 year NMPA requirements
Type: Full-time
Benefits: Comprehensive healthcare, professional development, family support, and equity opportunities

Parexel

Skills & Focus: Clinical Research, Site Management, Feasibility, Regulatory Compliance, Patient Recruitment, Training, Problem Solving, Project Management, Audit Readiness, Clinical Trials

Biomarin Pharmaceutical Inc.

Skills & Focus: Regulatory Affairs, Japanese regulatory, submissions, biotechnology, pharmaceutical, JNDA, negotiation, strategy, clinical development, communication skills
Experience: Minimum of ten years of industry experience with at least six years of experience in Regulatory Affairs in the biotechnology or pharmaceutical industries
Type: Full-Time

Biomarin

Skills & Focus: Regulatory Affairs, Japan, MHLW, PMDA, JNDAs, pharmaceutical, biotechnology, regulatory submissions, clinical development, strategic planning
About the Company: BioMarin is a biotechnology company specializing in developing innovative biopharmaceuticals for serious diseases and medical conditions.
Experience: Minimum of ten years of industry experience with at least six years of experience in Regulatory Affairs.
Type: Full-Time

Parexel

Skills & Focus: Client Relationship, Director, Sales, Account Management, Japan, Clinical Research, Biostatistics, Data Management, Operational Leadership, Patient Focused

Iqvia

Skills & Focus: CRA, clinical trials, monitoring, GCP, pharmaceutical, medical devices, reporting, Oncology, CNS, global studies
About the Company: IQVIA is a leading global provider of advanced analytics, technology solutions and clinical research services to the life sciences industry. We believe in push…
Experience: At least 1 year experience as CRA
Type: Full time
Benefits: Benefits programs are designed to meet your total well-being needs so you can thrive at work and at home.

Intuitive Surgical

Skills & Focus: clinical research, engineering leadership, medical devices, robotic systems, clinical studies, product development, regulatory compliance, patient safety, prototype evaluation, team management
About the Company: At Intuitive, we are united behind our mission: we believe that minimally invasive care is life-enhancing care. Through ingenuity and intelligent technology, w…
Experience: 10+ years in medical device development, 5+ years in leadership
Type: Full-time

Stryker

Skills & Focus: marketing strategies, customer engagement, product features, strategic planning, competitive dynamics, sales tools, KPI reporting, clinical evidence, interpersonal skills, analytical support
About the Company: Stryker offers innovative products and services in MedSurg, Neurotechnology and Orthopaedics that help improve patient and healthcare outcomes. Alongside its c…
Experience: 4+ years of work experience required; 2+ years medical device or marketing experience preferred
Type: Full Time
Benefits: Health benefits include medical and prescription drug insurance, dental insurance, vision insurance, critical illness i…

Veeva Systems

Skills & Focus: multichannel strategy, stakeholder management, pharmaceutical industry, data management, content delivery, healthcare professionals, sales collaboration, product expertise, efficiency, information delivery
About the Company: Veeva Systems is a mission-driven organization and pioneer in industry cloud, helping life sciences companies bring therapies to patients faster. As one of the…
Benefits: Work Anywhere

Pfizer

Skills & Focus: Customer Engagement Training, Brand / Business Unit, Therapeutic Area, Product Knowledge, Market Dynamics, Sales Techniques, Training Development, Stakeholder Management, Cross-Functional Collaboration, Digital Competencies
Experience: About 3 years of successful experience in sales, training, marketing, or related roles in Oncology
Type: Full-time

Boston Scientific

Skills & Focus: clinical training, electrophysiology, APAC, education strategies, training programs, medical solutions, procedures, cross-cultural collaboration, content development, training evaluation
About the Company: A leader in medical science committed to solving important health industry challenges with innovative medical solutions.
Experience: At least 10 years in cardiac electrophysiology and education roles

Regeneron

Skills & Focus: Field Medical, Oncology, Clinical Trials, Healthcare Professionals, Scientific Exchange, Therapeutic Area Expertise, Compliance, Data Presentation, Medical Affairs, Investigator-Initiated Studies
About the Company: Regeneron is a biotechnology company that discovers, develops, and commercializes innovative medicines for the treatment of serious diseases.
Experience: 3+ years of relevant experience in a pharmaceutical industry or clinical setting
Type: Contract
Benefits: Health and wellness programs, fitness centers, equity awards, annual bonuses, paid time off

Iqvia

Skills & Focus: HEOR, Clinical Research, Real World Evidence, Healthcare consulting, Life Sciences, Project Management, Data Analysis, Communication Skills, Team leadership, Statistical Analysis
About the Company: IQVIA is a leading global provider of clinical research services, commercial insights and healthcare intelligence to the life sciences and healthcare industrie…
Type: Full time
Benefits: Benefits programs are designed to meet your total well-being needs so you can thrive at work and at home.

Stryker

Skills & Focus: regulatory strategies, advocacy activities, product lifecycle, regulatory classification, compliance activities, regulatory submissions, quality data, clinical data, GCP inspections, project management
About the Company: Stryker is a global leader in medical technologies and, together with its customers, is driven to make healthcare better. The company offers innovative product…
Experience: Typically a minimum of 4 years’ experience
Type: Full Time
Benefits: bonuses, healthcare, insurance benefits, retirement programs, wellness programs, service and performance awards

Shockwave Medical

Skills & Focus: marketing strategy, brand strategy, sales promotion, evidence needs, training programs, medical education, product development, market assessments, KOL management, cross-functional collaboration
About the Company: Shockwave Medical is dedicated to providing better calcification treatment products to healthcare professionals worldwide, driven by an endless passion for inn…
Experience: 5+ years in cardiovascular marketing
Type: Full-time

Boston Scientific

Skills & Focus: clinical training, electrophysiology, APAC, medical solutions, training program, global collaboration, product launches, education excellence, procedures, medical solutions
About the Company: A leader in medical science for more than 40 years, committed to solving health industry challenges through innovative medical solutions.
Experience: Minimum undergraduate degree with at least 10 years of relevant experience in cardiac electrophysiology and education roles

Astrazeneca

Skills & Focus: program ownership, strategic direction, clinical trial management, drug development, regulatory environments, program budget, team effectiveness, clinical development, project management, cross-functional collaboration
About the Company: AstraZeneca is a global, science-led biopharmaceutical company that focuses on the discovery, development, and commercialization of prescription medicines. Its…
Experience: Minimum of eight (8) years of experience in drug development in pharmaceuticals, biopharmaceuticals, or biotechnology.
Type: Full-time

Biomarin Pharmaceutical Inc.

Skills & Focus: Regulatory Affairs, Japan, JNDA, submissions, pharmaceutical, biotechnology, strategic planning, post-marketing maintenance, regulatory authorities, collaborative skills
Experience: Minimum of ten years of industry experience with at least six years of experience in Regulatory Affairs in the biotechnology or pharmaceutical industries.
Type: Full-Time

Novartis

Skills & Focus: regulatory writing, clinical documentation, business management, quality control, clinical study reports, technical documents, coaching, mentoring, auditing, compliance
About the Company: Novartis is an innovative medicines company, working to reimagine medicine to improve and extend people’s lives. Our medicines reach more than 250 million peop…

Psi

CRA II Tokyo
Skills & Focus: clinical research, monitoring visits, study startup, CRF review, source document verification, query resolution, budget negotiations, trial progress monitoring, site communication, feasibility research
About the Company: PSI is a full-service global clinical research organization (CRO) that focuses on clinical research projects across various therapeutic indications.
Type: Full-time

Primevigilance

Skills & Focus: project management, client relations, quality assurance, training, coordination, milestones, reporting, invoicing, pharmacovigilance, team leadership
About the Company: PrimeVigilance is a leading provider of pharmacovigilance services, specializing in managing the safety of pharmaceutical products through rigorous monitoring …
Experience: 5+ years in project management or related fields
Salary: Competitive
Type: Full-time
Benefits: Health insurance, paid time off, and professional development opportunities

Biomarin Pharmaceutical Inc.

Skills & Focus: contracts administration, contract management, pharmaceutical, biotechnology, legal, corporate compliance, regulatory affairs, Non-Disclosure Agreements, Clinical Trial Agreements, contract lifecycle management
Experience: A minimum of 3 years’ experience in contracts administration or other relevant work experience.
Type: Full-Time

Psi

Skills & Focus: clinical studies, stakeholder communication, site monitoring, CRF review, source document verification, query resolution, project timelines, feasibility research, site audits, study submissions
About the Company: Join the PSI team and help drive innovation and excellence in advancing healthcare solutions.
Experience: Experience in clinical studies, site monitoring, and project management

Biomarin

Skills & Focus: Contract Management, Legal Department, Contracts, Non-Disclosure Agreements, Master Service Agreements, Clinical Trial Agreements, Compliance, Pharmaceutical, Business Communication, Organizational Skills
About the Company: BioMarin is a high-performing, team-based organization specializing in pharmaceutical and biotechnology compliance.
Experience: A minimum of 3 years’ experience in contracts administration or other relevant work experience.
Type: Full-Time

Primevigilance

Skills & Focus: case processing, Individual Case Safety Reports, pharmacovigilance, SAE/SUSAR Management, clinical trials, post-marketing, database outputs, mentoring, training, procedure optimization
About the Company: PrimeVigilance is a pharmacovigilance service provider that specializes in managing case processing for clinical trials and post-marketing surveillance.
Experience: Demonstrated experience in case processing
Type: Full-time

Intuitive Surgical

Skills & Focus: Regulatory, Medical Devices, Global Regulatory Intelligence, EU MDR, clinical evaluation, Product claims, Regulatory submissions, EU Notified Body, Advertising and Promotion, Regulatory Trends
About the Company: At Intuitive, we are united behind our mission: we believe that minimally invasive care is life-enhancing care. Through ingenuity and intelligent technology, w…
Experience: 10+ years
Type: Full-time

Biogen

Skills & Focus: medical leadership, strategic direction, cross-functional team, medical plans, stakeholder engagement, patient needs, medical education, scientific relationships, Japan affiliate, Biogen portfolio

Stryker

Skills & Focus: marketing, sales, medical education, program design, interpersonal skills, data management, budgeting, communication, project management, analytical skills
About the Company: Stryker offers innovative products and services in MedSurg, Neurotechnology, and Orthopaedics that help improve patient and healthcare outcomes.
Experience: 2+ years of work experience required
Type: Full Time
Benefits: Healthcare, insurance benefits, retirement programs, wellness programs, performance awards, and various social and recr…

Syneos Health

Skills & Focus: scientific strategies, drug development, medical affairs, collaboration, communication skills, FDA regulations, business acumen, cross functional solutions, biopharma industry, patient focus
About the Company: Syneos Health® is a leading fully integrated biopharmaceutical solutions organization built to accelerate customer success. Every day we perform better because…
Experience: MD or PhD or equivalent and significant experience in drug development experience within the biopharma or CRO industry.
Type: Full-time
Benefits: We are passionate about developing our people, through career development and progression; supportive and engaged line …

Intuitive Surgical

Skills & Focus: regulatory, medical devices, EU MDR, clinical evaluation, CE marking, global markets, regulatory submissions, compliance, regulatory intelligence, product portfolio
About the Company: At Intuitive, we are united behind our mission: we believe that minimally invasive care is life-enhancing care. Through ingenuity and intelligent technology, w…
Experience: 10+ years
Type: Full-time

Novartis

Skills & Focus: regulatory strategies, drug development, marketing authorization, post marketing products, Japanese labeling, cross functional communication, regulatory activities, MHLW/PMDA, adverse events, mentorship
About the Company: Novartis is an innovative medicines company. Every day, we work to reimagine medicine to improve and extend people’s lives.
Experience: Train and mentor RA members concerning drug development. Understand varied knowledge of Japan regulation.
Type: Full-time

Veeva Systems

Skills & Focus: life sciences, commercial strategies, content management, business consulting, customer engagement, marketing, medical content, project leadership, subject matter expertise, innovative environment
About the Company: Veeva Systems is a mission-driven organization and pioneer in industry cloud, helping life sciences companies bring therapies to patients faster. As one of the…
Experience: Strong management consulting or agency experience; understanding of commercial content operations processes, tools, and systems.
Type: Full-time
Benefits: Flexible work from home or in the office.

Iqvia

Skills & Focus: Medical Writing, Clinical Trials, Regulatory Documentation, Pharmaceuticals, GCP, ICH Guidelines, Multilingual Documentation, Clinical Research, Quality Control, Medical Knowledge
About the Company: IQVIA is a leading global provider of clinical research services, commercial insights and healthcare intelligence to the life sciences and healthcare industrie…
Experience: Experience in Medical Writing
Type: Full time
Benefits: Benefits programs are designed to meet your total well-being needs.

Ergomed

Skills & Focus: pharmacovigilance, case processing, Individual Case Safety Reports, SAE/SUSAR submissions, regulatory requirements, PBRER, DSUR, PADER, mentoring, continuous improvement

Boston Scientific

Skills & Focus: Electrophysiology, Ablation technologies, Mapping platforms, Pulsed field ablation, Clinical trials, Research collaborations, Product development, Data analysis, APAC travel, Medical solutions
About the Company: Boston Scientific is a global leader in medical science, committed to solving health challenges and transforming lives through innovative solutions.
Experience: Minimum 3 years in field or research with EP technologies

Pfizer

Skills & Focus: medical strategy, medical plan, medical & scientific communication, KOLs, clinical development, medical affairs, oncology, therapeutic area, medical information, regulations
Type: Full time