58 Biopharmaceutical Leadership jobs in Tokyo.

Tokyo

• Skills: life sciences, commercial strategies, content management, business consulting, customer engagement, marketing, medical content, project leadership, subject matter expertise, innovative environment
• Experience: Strong management consulting or agency experience; understanding of commercial content operations processes, tools, and systems.
• Type: Full-time

Tokyo

• Skills: project management, client relations, quality assurance, training, coordination, milestones, reporting, invoicing, pharmacovigilance, team leadership
• Experience: 5+ years in project management or related fields
• Type: Full-time

Tokyo

• Skills: clinical research, monitoring visits, study startup, CRF review, source document verification, query resolution, budget negotiations, trial progress monitoring, site communication, feasibility research
• Type: Full-time

Tokyo

• Skills: Contract Management, Legal Department, Contracts, Non-Disclosure Agreements, Master Service Agreements, Clinical Trial Agreements, Compliance, Pharmaceutical, Business Communication, Organizational Skills
• Experience: A minimum of 3 years’ experience in contracts administration or other relevant work experience.
• Type: Full-Time

Tokyo

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

Tokyo

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

Tokyo

• Skills: clinical operations, project leader, clinical trials, team management, global research operations, project planning, customer interaction, project execution, responsibility, interdisciplinary coordination
• Experience: 5+ years of experience in clinical development (including CRA/PM/PL experience)

Tokyo

• Skills: HEOR, Clinical Research, Real World Evidence, Healthcare consulting, Life Sciences, Project Management, Data Analysis, Communication Skills, Team leadership, Statistical Analysis
• Type: Full time

Tokyo

• Skills: Regulatory Affairs, approval applications, medical devices, PMDA consultations, QMS compliance, certification, communication, project management, healthcare outcomes, medical insurance
• Experience: 3+ years of experience of medical device (Class I to IV) application approvals
• Type: Full Time

Tokyo

• Skills: CRA, clinical trials, monitoring, GCP, pharmaceutical, medical devices, reporting, Oncology, CNS, global studies
• Experience: At least 1 year experience as CRA
• Type: Full time

Tokyo

• Skills: regulatory writing, clinical documentation, business management, quality control, clinical study reports, technical documents, coaching, mentoring, auditing, compliance

Tokyo

• Skills: Field Medical, Oncology, Clinical Trials, Healthcare Professionals, Scientific Exchange, Therapeutic Area Expertise, Compliance, Data Presentation, Medical Affairs, Investigator-Initiated Studies
• Experience: 3+ years of relevant experience in a pharmaceutical industry or clinical setting
• Type: Contract

Tokyo

• Skills: 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

Tokyo

• Skills: clinical trials, study start-up, budget execution, clinical study execution, site-level goal setting, vendor management, country strategy, regulatory knowledge, team collaboration, risk mitigation
• Experience: Doctorate degree OR Master’s degree & 3 years of directly related experience OR Bachelor’s degree & 5 years of directly related experience OR Associate’s degree & 10 years of directly related experience.
• Type: Full time

Tokyo

• Skills: Regulatory, Medical Devices, Global Regulatory Intelligence, EU MDR, clinical evaluation, Product claims, Regulatory submissions, EU Notified Body, Advertising and Promotion, Regulatory Trends
• Experience: 10+ years
• Type: Full-time

Tokyo

• Skills: regulatory intelligence, regulatory strategy, product lifecycle, market access, regulatory compliance, clinical research, regulatory submissions, cross-functional teams, GCP inspections, document compliance
• Type: full_time

Tokyo

• Skills: regulatory management, Japan regulation, MHLW, PMDA, drug development, regulatory strategies, submission and approval, cross functional communication, post-marketing products, labeling
• Type: full_time

Tokyo

• Skills: Regulatory submissions, Clinical trials, PMDA, Life Sciences, Medicine, Pharmacy, Regulatory environment, Bilingual, Training, Documentation
• Type: full_time

Tokyo

• Skills: Regulatory strategy, Drug development, Medical devices, Regulatory submissions, Health Authority, MHLW/PMDA, Interpersonal skills, Bilingual communication, Project management, Problem solving

Tokyo

• Skills: Oncology, Medical Affairs, Compliance, Pharmaceutical, Leadership, Stakeholder Engagement, Drug Development, Health Economics, Regulatory, Cross-functional Collaboration
• Type: full_time