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Safety & Pv Specialist I (Japanese Language Expert)

0-2 years
₹6,00,000 – ₹8,00,000 per annum
10 Aug. 13, 2025
Job Description
Job Type: Full Time Education: M.Sc./M.Pharm/PhD 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

Safety & PV Specialist I (Japanese Language Expert)
Location: Gurugram, India

Company Overview:
Syneos Health® is a global leader in fully integrated biopharmaceutical solutions, working to accelerate customer success by translating clinical, medical affairs, and commercial insights into real-world outcomes. With over 29,000 employees across 110 countries, the organization prioritizes simplifying processes, fostering collaboration, and ensuring agility in delivering therapies to patients worldwide.

Why Join Syneos Health:

  • Career development and progression opportunities.

  • Supportive and engaged line management.

  • Technical and therapeutic area training.

  • Peer recognition and total rewards program.

  • Inclusive “Total Self” culture that embraces diversity and authenticity.

Key Responsibilities:

  • Enter data into PVG quality and tracking systems for ICSR receipt and tracking.

  • Assist in processing ICSRs per SOPs and project-specific safety plans.

  • Triages and evaluates ICSR data for completeness, accuracy, and regulatory reporting.

  • Code events, medical history, medications, and tests in safety databases.

  • Compile narrative summaries and follow up on outstanding queries.

  • Generate timely and accurate expedited safety reports per regulations.

  • Maintain safety tracking systems and perform literature screening for safety data.

  • Conduct MedDRA coding and manage drug dictionaries.

  • Validate and submit xEVMPD product records, coding indications appropriately.

  • Manage duplicate ICSRs and perform quality review of case reports.

  • Handle SPOR/IDMP-related activities.

  • Ensure TMF and PSMF document submission compliance.

  • Stay updated with SOPs, regulatory guidelines (GCP, ICH, GVP), and project plans.

  • Foster professional relationships with internal and external teams.

  • Participate in audits as required.

Qualifications:

  • Master’s degree in Pharmacy (preferred) or Master’s in Science/Healthcare, or equivalent experience.

  • Strong interpersonal and communication skills.

  • Advanced Microsoft Office proficiency.

  • Japanese language proficiency essential for role.

Salary Range: ₹6,00,000 – ₹8,00,000 per annum (estimated industry standard for role and location).