Patient Safety Associate II / Patient Safety Specialist – Japanese Language
Location: India (Remote)
Job ID: R0000035627
Category: Medical Sciences / Pharmacovigilance
Employment Type: Full-time
About the Role
Parexel is seeking a highly motivated Patient Safety Associate II / Patient Safety Specialist (Japanese-speaking) to support global pharmacovigilance and drug safety operations. This remote role, based in India, is ideal for professionals with strong expertise in ICSR case processing, global safety reporting, Japanese PV regulations (PMDA), and end-to-end safety lifecycle management.
The role requires close collaboration with global clients, regulatory authorities, and internal stakeholders to ensure compliance with international drug safety regulations while delivering high-quality patient safety outcomes.
Key Responsibilities
General Patient Safety Activities
Maintain in-depth knowledge of assigned products’ safety profiles, labeling, SOPs, and global pharmacovigilance regulations
Ensure compliance with global regulatory reporting timelines and internal quality standards
Assist in developing project-specific safety workflows, procedures, and templates
Participate in internal, client, and project-specific drug safety training programs
Support audit and inspection readiness, including follow-up actions
Monitor client-defined performance metrics and maintain compliance targets
Mentor junior team members and support onboarding activities
Liaise with client stakeholders to ensure timely, accurate, and high-quality deliverables
Case Processing & Safety Data Management
Monitor and triage incoming safety reports from multiple sources including literature, EudraVigilance, and mailboxes
Perform completeness, validity, and medical consistency checks on safety reports
Create and process cases in safety databases with accurate data entry as per SOPs
Conduct MedDRA coding in line with “MedDRA Term Selection: Points to Consider”
Assess seriousness, causality, and expectedness of adverse events
Prepare medically coherent case narratives and manage follow-up queries
Perform quality control, reconciliation, and compliance checks for ICSRs
Support generation of line listings, tabulations, and periodic safety reports
Drug Safety Reporting & Regulatory Compliance
Perform quality control of safety reports and expedited submissions
Support electronic and non-electronic submissions to global Health Authorities
Track, reconcile, and archive submitted safety cases and documentation
Assist with SUSAR unblinding and safety information dissemination
Collaborate on compliance metrics, late case investigations, and corrective actions
Regulatory Affairs & Database Management
Maintain and update regulatory databases for product lifecycle changes
Support xEVMPD submissions and tracking via EMA Gateway
Create regulatory events, variations, and reports for EU and global submissions
Validate regulatory data against SmPC and labeling documents
Literature Search & Review
Develop and maintain literature search strategies aligned with client requirements
Perform local and global literature surveillance and quality checks
Identify valid safety cases and enter them into safety databases
Maintain and update local journal lists and search strategies
Required Skills & Competencies
Strong knowledge of pharmacovigilance processes and global safety regulations
Experience in ICSR processing, safety databases, and compliance reporting
Excellent analytical, problem-solving, and organizational skills
Strong interpersonal and stakeholder management abilities
Proficiency in MS Office and web-based PV systems
Ability to manage multiple priorities with attention to detail
Language & Regional Expertise
Fluent English and Japanese (written and spoken)
JLPT N2 or higher certification (mandatory)
Hands-on experience with PMDA pharmacovigilance activities
Experience working with Japanese-speaking PV teams preferred
Education
Degree in Life Sciences, Pharmacy, Biomedical Sciences, Biotechnology, Microbiology, or related field
Medical, Nursing, Dentistry, Physiotherapy, or patient-facing clinical degrees are an added advantage
Experience Required
2–6 years of relevant experience in Pharmacovigilance / Drug Safety / Patient Safety
Prior experience in Japanese PV case processing and global safety reporting is highly desirable
Why Join Parexel
Parexel offers an inclusive, globally connected work environment where patient safety and scientific excellence drive every decision. This role provides the opportunity to work on international projects, collaborate with global regulatory bodies, and contribute meaningfully to patient health outcomes—while working remotely from India.
Keywords for SEO & GEO Optimization:
Patient Safety Specialist Jobs, Pharmacovigilance Jobs India, Japanese PV Jobs, Drug Safety Associate, ICSR Case Processing, PMDA Pharmacovigilance, Remote PV Jobs, Parexel Careers, Global Patient Safety Roles
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