21 Clinical Operations Management jobs in Tokyo.

Hiring now: Study Ops Mgr Spain Fsp @ Parexel, Medical Scientific Mgr @ Biomarin P, Rwe Clinical Proj Mgr @ Iqvia, Pv Officer @ Primevigil, Sr Clinical Trial Mgr @ Syneos Hea, Regulatory Affairs Mgr Sr @ Amgen, Sr Medical Science Liaiso @ Astrazenec, Clinical Science Liaison @ Boston Sci, Cra Ii @ Psi.Explore more at jobswithgpt.com.

🔥 Skills

Clinical Research (6) Clinical Trials (5) project management (5) CRA (4) Project Management (4) clinical trials (4) training (4) GCP (3) quality assurance (3) Oncology (3)

📍 Locations

Tokyo (21)

Parexel

Skills & Focus: Clinical Research, FSP, Remote, CRA, Biostatisticians, Clinical Trials, Project Leaders, Data Managers, Regulatory Consultants, Statistical Programmers
Skills & Focus: Clinical Research Associate, CRA, SSU, Management, Monitoring, Patient safety, Project assignment, Team leadership, Coaching, Cross-functional collaboration
About the Company: Parexel is a global biopharmaceutical services organization that accelerates the development of innovative therapies and enables the successful commercializati…
Experience: 3 years of experience in CRA/SSU management

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, 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: Clinical Lead, Project Lead, Clinical Operation, Monitoring Lead, Data Collection, Project Management, RFP, Budget Management, Timelines, Risk Management
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.

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

Syneos Health

Skills & Focus: clinical monitoring, data integrity, protocol compliance, risk management, site management, central monitoring, clinical trial, investigator interactions, training, budget management
About the Company: Syneos Health® is a leading fully integrated biopharmaceutical solutions organization built to accelerate customer success. We translate unique clinical, medic…
Experience: Bachelor’s degree or RN in a related field or equivalent combination of education, training, and experience
Type: Hybrid

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.

Syneos Health

Skills & Focus: Safety Management, Pharmacovigilance, Project Management, Clinical Research, Staff Management, Budget Reviews, Regulatory Compliance, Data Protection, Process Development, Team Leadership
About the Company: Syneos Health® is a leading integrated biopharmaceutical solutions organization built to accelerate customer success. We translate unique clinical, medical aff…
Experience: Progressive responsibility with demonstrated leadership skills and project management.
Type: Hybrid

Amgen

Skills & Focus: Regulatory Affairs, Japan, clinical trials, marketing licenses, drug development, regulatory submissions, PMDA, NDA, Orphan Drug Applications, cross-functional teams
Experience: 10+ years including 5+ years in Regulatory Affairs
Type: Full time
Skills & Focus: Post Marketing Surveillance, project management, PMS activities, regulatory compliance, data management, process improvement, budget management, collaboration, quality assurance, training
Type: Full time

Astrazeneca

Skills & Focus: oncology, MSL, relationship management, project management, medical affairs, stakeholder management, scientific expertise, clinical trials, strategic planning, cross-functional collaboration
About the Company: AstraZeneca is one of the world’s most forward-thinking and connected BioPharmaceutical companies, dedicated to helping patients by delivering life-changing me…
Experience: 3+ years in oncology or MSL experience

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.

Boston Scientific

Skills & Focus: Clinical Science Liaison, Interventional Oncology, Clinical Trials, Patient Recruitment, Site Management, Medical Insights, Data Quality, GCP, Oncology, Research Support
Experience: 業界の医療または臨床の役割で5年以上の経験
Salary: 年収 約1100万円まで
Type: Hybrid
Benefits: ボーナス年1回3月支給、固定残業代55時間/月を含む

Astrazeneca

Skills & Focus: medical affairs, clinical research, stakeholder management, project management, oncology, evidence generation, regulatory knowledge, team management, communication skills, compliance
About the Company: AstraZeneca is one of the world’s most forward-thinking and connected BioPharmaceutical companies, dedicated to helping patients by delivering life-changing me…
Experience: 3+ years in medical affairs or development in the pharmaceutical industry
Skills & Focus: Oncology, Medical Affairs, Clinical Research, Project Management, Communication Skills, Stakeholders, Evidence Generation, Regulatory Knowledge, Scientific Writing, Team Management
About the Company: AstraZeneca is one of the world’s most forward-thinking and connected BioPharmaceutical companies.
Experience: 3+ years in oncology clinical or medical experience
Skills & Focus: clinical delivery, project management, operational delivery, clinical studies, vendor contracts, monitoring, risk management, quality assurance, team building, ICH-GCP
About the Company: AstraZeneca is one of the world’s most forward-thinking and connected BioPharmaceutical companies.
Experience: At least 5 years’ experience from within the pharmaceutical industry or similar organization or academic experience.

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

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