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Safety Specialist Ii

0-2 years
Not Disclosed
10 May 28, 2025
Job Description
Job Type: Full Time Education: B.Sc./M.Sc/B.Pharm/M.Pharm/Life Science 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: Safety Specialist II


Job Overview

We are currently seeking a Safety Specialist II to join our growing team at Navitas Life Sciences. This role involves the preparation and review of aggregate safety reports, signal management, and contributions to risk management activities. The ideal candidate will have a strong understanding of pharmacovigilance principles, regulatory guidelines, and the ability to work collaboratively across cross-functional teams.


Key Responsibilities

Aggregate Safety Reports

  • Author and review aggregate reports such as:

    • DSURs (Development Safety Update Reports)

    • PBRERs (Periodic Benefit-Risk Evaluation Reports)

    • PSURs (Periodic Safety Update Reports)

    • PADERs (Periodic Adverse Drug Experience Reports)

    • Canadian Aggregate Reports

  • Review safety data and generate line listings (LL) and summary tabulations (ST) using safety databases

  • Analyze safety and regulatory data provided by clients and compile complete reports per specifications

  • Perform literature screening to include relevant safety articles in the appropriate report sections

  • Incorporate benefit-risk evaluations provided by medical reviewers

  • Ensure adherence to internal/external timelines and client-specific requirements

  • Address reviewer comments and finalize reports for submission

  • Support and participate in internal/external audits and health authority inspections

Signal Management & Risk Management Plans

  • Conduct signal screening, data mining, and frequency tabulations for potential safety signals

  • Generate LL & ST from safety databases (e.g., Argus/client-specific systems)

  • Draft documents for signal detection, validation, assessment, and benefit-risk analysis

  • Ensure compliance with SOPs, conventions, and pharmacovigilance guidelines

  • Track signal status: potential, validated, refuted, open, or closed

  • Assist in the development and authoring of Risk Management Plans (RMPs) in accordance with SOPs


Required Experience & Qualifications

Technical & Domain Knowledge

  • Proven ability to author and review aggregate safety reports

  • Experience specifically with PBRERs and other global safety reports

  • Working knowledge of medical and pharmacovigilance terminology

  • Strong familiarity with GCP, GVP, ICH, USFDA, and other relevant PV guidelines

  • Competent in using MS Office tools (Word, Excel, PowerPoint)

Cross-functional Support

  • Ability to assist the Individual Case Safety Report (ICSR) team and Literature Review team based on workload

  • Help in scheduling and planning of report assignments

Soft Skills

  • High motivation and excellent communication skills

  • Structured, organized, and reliable approach to work

  • Strong team orientation and commitment

  • Ability to work under pressure and meet deadlines

  • Proficiency in written and spoken English (additional languages are a plus)