Last updated: 2025-05-22

12 Clinical Operations Management jobs in Tokyo.

Hiring now: Fsp Clinical Research Ass @ Parexel, Medical Scientific Mgr @ Biomarin P, Post Mktg Surveillance Pm @ Amgen, Cra 臨床開発モニター @ Iqvia, Cra Ii @ Psi, Pv Proj Mgr @ Primevigil.Explore more at at kaamvaam.com

🔥 Skills

Clinical Research (4) Clinical Trials (4) CRA (3) clinical trials (3) training (3) global studies (2) collaboration (2) Project Management (2) Data Management (2) Regulatory Compliance (2)

📍 Locations

Tokyo (12)

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

Amgen

Skills & Focus: Post Marketing Surveillance, project management, PMS activities, regulatory compliance, data management, process improvement, budget management, collaboration, quality assurance, training
Type: Full time

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

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.

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

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

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.