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Drug Safety Specialist - Japanese

Parexel
Parexel
2-6 years
preferred by company
10 Dec. 22, 2025
Job Description
Job Type: Full Time Remote Education: B.Sc./ M.Sc./ M.Pharm/ B.Pharm/ Life Sciences Skills: Causality Assessment, Clinical SAS Programming, Communication Skills, CPC Certified, GCP guidelines, ICD-10 CM Codes, CPT-Codes, HCPCS Codes, ICD-10 CM, CPT, HCPCS Coding, ICH guidelines, ICSR Case Processing, Interpersonal Skill, Labelling Assessment, MedDRA Coding, Medical Billing, Medical Coding, Medical Terminology, Narrative Writing, Research & Development, Technical Skill, Triage of ICSRs, WHO DD Coding

Drug Safety Specialist – Japanese Language (Pharmacovigilance)

Location: India (Remote)
Employment Type: Full-Time
Industry: Pharmaceutical & Life Sciences
Functional Area: Medical Sciences / Pharmacovigilance
Experience Required: 2–6 Years (Drug Safety / PV preferred)
Language Requirement: Japanese (JLPT N2 or above) + English


Job Overview

We are seeking a highly skilled Drug Safety Specialist – Japanese to support global pharmacovigilance operations with a strong focus on Japanese regulatory requirements and PMDA safety reporting. This role involves end-to-end case processing, safety reporting, regulatory compliance, and literature surveillance for investigational and marketed products.

The position is ideal for professionals with hands-on pharmacovigilance experience, Japanese language proficiency, and exposure to global safety databases and reporting workflows.


Key Responsibilities

General Pharmacovigilance Activities

  • Maintain in-depth knowledge of assigned products’ safety profiles, labeling, client SOPs, and global drug safety regulations

  • Ensure compliance with global and local adverse event reporting timelines

  • Support development of project-specific safety workflows, templates, and procedures

  • Participate in and conduct internal, client, and project-specific PV training sessions

  • Prepare for, participate in, and follow up on audits and regulatory inspections

  • Monitor performance metrics and ensure adherence to client-defined quality benchmarks

  • Delegate and review work performed by Drug Safety Assistants

  • Collaborate with client stakeholders to ensure timely, high-quality deliverables

  • Mentor and support onboarding of new team members

  • Ensure proper archiving of source documents and safety correspondence


Case Processing & ICSR Management

  • Monitor incoming safety reports from multiple sources (mailboxes, EudraVigilance, literature, affiliates)

  • Perform triage and validation of cases for completeness, validity, and medical coherence

  • Create and process cases within the safety database with accurate data entry

  • Perform MedDRA coding in compliance with MedDRA Points to Consider

  • Assess seriousness, causality, and expectedness of adverse events

  • Prepare medically sound and cohesive case narratives

  • Manage follow-up requests and query resolution

  • Conduct case reconciliation with Data Management teams

  • Generate line listings and tabulations for periodic and ad-hoc safety reports

  • Support compliance activities for late ICSRs and contribute to root cause analysis and corrective actions


Drug Safety Reporting & Compliance

  • Perform quality control checks on case reports, listings, and tabulations

  • Support expedited reporting processes and local safety reporting requirements

  • Coordinate electronic and paper submissions to regulatory authorities, ethics committees, and investigators

  • Manage SUSAR unblinding activities when required

  • Track safety submissions and maintain documentation

  • Generate, monitor, and reconcile compliance metrics with internal and external stakeholders


Regulatory Affairs & Database Management

  • Compare client-provided regulatory data with internal databases and remediate gaps

  • Maintain lifecycle changes for medicinal products in regulatory systems

  • Create regulatory events, variations, and references for EU and global procedures

  • Support PSUSA, PBRER, referrals, and labeling updates

  • Perform xEVMPD submissions via EMA Gateway and track acknowledgements

  • Generate marketing authorization and PV coordination reports


Literature Search & Review

  • Develop and maintain literature search strategies per client requirements

  • Conduct local and global literature surveillance and data entry of valid cases

  • Maintain local journal lists and update search strategies as required

  • Perform quality checks on search outputs and strategy updates

  • Coordinate with internal and external stakeholders to resolve literature-related issues


Required Skills & Competencies

  • Strong knowledge of pharmacovigilance and drug development processes

  • Ability to interpret and apply global safety regulations

  • Experience in safety data analysis and evaluation

  • Proficiency in safety databases and literature search tools

  • Excellent analytical, organizational, and problem-solving skills

  • Strong written and verbal communication skills

  • Ability to manage multiple priorities with high attention to detail

  • Client-focused mindset with strong collaboration skills

  • Proficiency in MS Office and web-based PV systems


Language & Regional Expertise

  • Japanese language proficiency: JLPT N2 or higher (mandatory)

  • Strong written and spoken English

  • Experience with PMDA pharmacovigilance activities preferred

  • Prior experience working with Japanese-speaking PV teams is an advantage


Education Requirements

  • Bachelor’s or Master’s degree in Life Sciences, Pharmacy, Biomedical Sciences, Biotechnology, Microbiology, Biochemistry, or related fields

  • Degrees involving clinical exposure (Medicine, Nursing, Dentistry, Physiotherapy, Experimental Medicine) are an added advantage


Why Join This Role

This role offers exposure to global pharmacovigilance operations, Japanese regulatory systems, and end-to-end safety reporting, making it ideal for professionals seeking growth in international drug safety, regulatory compliance, and client-facing PV roles.


Disclaimer

This job description outlines the general nature and level of responsibilities for this role and is not intended to be an exhaustive list. Responsibilities may evolve based on project and organizational requirements.