Last updated: 2025-05-22

17 Clinical Data And Biostatistics jobs in Tokyo.

Hiring now: Site Technology Spec @ Psicro, Fsp Clinical Research Ass @ Parexel, Medical Scientific Mgr @ Biomarin P, Pv Associate @ Ergomed, Sr Mgr International Regu @ Biomarin, Cra 臨床開発モニター @ Iqvia, Sr Mgr Field Medical Affa @ Regeneron, Scientific Implementation @ Uncountabl, Cra Ii @ Psi, Pv Officer @ Primevigil.Explore more at at kaamvaam.com

🔥 Skills

Clinical Research (5) Clinical Trials (5) clinical trials (4) CRA (3) Project Management (3) global studies (2) Data Management (2) Regulatory Compliance (2) Statistical Analysis (2) pharmacovigilance (2)

📍 Locations

Tokyo (17)

Psicro

Skills & Focus: clinical trial, technology, imaging, radiology, radionuclide, cell therapy, clinical trial sites, technologies, equipment qualification, data collection

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

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

Parexel

Skills & Focus: Clinical Research, Site Management, Feasibility, Regulatory Compliance, Patient Recruitment, Training, Problem Solving, Project Management, Audit Readiness, Clinical Trials
Skills & Focus: Clinical Research, CRA, Remote, FSP, Biostatistics, Statistical Programming, Clinical Trials, Data Management, Project Leadership, Functional Service Provider
About the Company: Parexel is a global biopharmaceutical services organization that provides a range of services to assist clients in the development of new therapies and in brin…
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

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.

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

Uncountable

Skills & Focus: scientific implementation, customer data, product development, data structuring, R&D, customer success, meetings and demos, scientific due diligence, platform configuration, performance bonus
Salary: 90-120K USD Per Year, in addition to performance bonus and equity

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.
Skills & Focus: analytics, consultant, healthcare, data analytics, project management, consulting, pharmaceuticals, market strategy, commercial excellence, real world data
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…
Type: Full time
Benefits: Benefits programs are designed to meet your total well-being needs so you can thrive at work and at home.

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
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

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

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.