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Drug Safety Specialist - Japanese

0-2 years
Not Disclosed
10 Sept. 25, 2025
Job Description
Job Type: Full Time Education: B.Sc/M.Sc/M.Pharma/B.Pharma/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

Job Title:

Drug Safety Specialist – Japanese

Location:

India (Remote)

Job ID:

R0000035627

Category:

Medical Sciences / Pharmacovigilance


About the Role:

The Drug Safety Specialist is responsible for ensuring high-quality pharmacovigilance (PV) activities for assigned drugs, maintaining compliance with global regulatory requirements, and supporting regulatory reporting obligations. This role includes case processing, drug safety reporting, regulatory affairs support, and literature review. Japanese language proficiency is required.


Minimum Qualifications & Experience:

  • Degree in Life Sciences, Health, or Biomedical Sciences (Pharmacy, Microbiology, Biochemistry, Biotechnology, Biophysics, etc.), or relevant PV experience.

  • Degrees in Medicine, Dentistry, Physiotherapy, Experimental Medicine, or Nursing are advantageous.

  • JLPT N2 or higher certification (Japanese language proficiency).

  • Knowledge of drug safety, pharmacovigilance regulations, and case processing.

  • Experience with Japanese-speaking PV case processing teams and PMDA PV activities is preferred.


Key Responsibilities:

General PV Duties:

  • Maintain knowledge of assigned drugs’ safety profile, labeling, client SOPs, and global PV regulations.

  • Organize work to comply with regulatory timelines and internal reporting standards.

  • Assist in development of project-specific PV procedures, workflows, and templates.

  • Attend/conduct internal and project-specific trainings.

  • Support audits and inspections preparation and follow-up.

  • Mentor new team members and delegate tasks to Drug Safety Assistants as needed.

  • Maintain archiving of source documents and relevant correspondence.

Case Processing:

  • Monitor incoming reports (mailboxes, Eudravigilance, literature searches).

  • Perform triage for completeness, legibility, and validity.

  • Ensure medical cohesiveness and data consistency.

  • Enter cases into safety databases accurately and perform quality checks.

  • Manage queries, follow-ups, and literature searches.

  • Prepare case narratives and support line listings and tabulation generation.

Drug Safety Reporting:

  • Quality control of case reports, line listings, and tabulations.

  • Maintain local and global drug safety reporting requirements.

  • Execute safety report submissions to investigators and regulatory authorities.

  • Perform unblinding of SUSARs as required.

  • Track and generate reporting compliance metrics.

Regulatory Affairs Support:

  • Maintain regulatory database information for medicinal products and devices.

  • Track lifecycle changes, variations, and label updates.

  • Perform xEVMPD submissions via EMA Gateway and track status.

  • Generate reports for dossier dispatch and marketing authorization updates.

Literature Search & Review:

  • Develop and maintain literature search strategies.

  • Identify, retrieve, and review scientific literature for valid case entry.

  • Maintain local journals in scope and perform quality checks on search strategies.

  • Implement updates to thesauri and resolve literature-related issues.


Skills & Competencies:

  • Strong knowledge of drug safety and pharmacovigilance processes.

  • Knowledge of global PV regulations and reporting requirements.

  • Analytical and problem-solving skills; ability to evaluate data independently.

  • Proficient in database management, literature searches, and Microsoft Office Suite.

  • Excellent verbal/written communication skills in English and Japanese.

  • Strong organizational, prioritization, and teamwork abilities.


Preferred Experience:

  • Prior experience in drug safety / pharmacovigilance roles.

  • Familiarity with medical terminology and regulatory submission processes.

  • Experience with Japanese PV regulations and case processing systems.