Welcome Back

Google icon Sign in with Google
OR
I agree to abide by Pharmadaily Terms of Service and its Privacy Policy

Create Account

Google icon Sign up with Google
OR
By signing up, you agree to our Terms of Service and Privacy Policy
Instagram
youtube
Facebook

Safety Systems Specialist

Fortrea
Fortrea
2+ years
preferred by company
Bangalore, India
1 May 12, 2026
Job Description
Job Type: Full Time Education: M.Pharm/B.Pharm or M.Sc. Skills: Medical Billing, Medical Coding, Medical Terminology, mRS and EQ-5D-5L., Narrative Writing, Research & Development, Technical Skill, Triage of ICSRs

Safety Systems Specialist | Pharmacovigilance Systems & Drug Safety Technology

Job Location: Bangalore, India
Job Type: Full-Time
Department: Clinical Safety / Pharmacovigilance Systems / Drug Safety Technology
Work Mode: Office-Based / Remote / Hybrid (As per business requirements)
Experience Required: 2+ Years
Freshers Eligible: No
Industry: Pharmacovigilance / Clinical Research / Pharmaceuticals / Life Sciences / Healthcare Technology

Job Overview

We are hiring a Safety Systems Specialist for a pharmacovigilance technology and drug safety systems role in Bangalore. This opportunity is ideal for professionals with experience in drug safety systems configuration, pharmacovigilance platform support, safety data migration, system validation, technical support, and clinical safety technology operations.

The selected candidate will support implementation, configuration, migration, reporting, issue resolution, and operational management of enterprise safety systems used in pharmacovigilance and clinical safety workflows.

This role is an excellent opportunity for professionals seeking career growth in drug safety technology, pharmacovigilance systems, clinical safety IT operations, and healthcare systems support.

Job Responsibilities

Safety Systems Operations

  • Support implementation, configuration, maintenance, and migration activities for drug safety and pharmacovigilance systems.
  • Perform project-specific configuration changes in safety platforms based on operational and client requirements.
  • Maintain and document system configurations, updates, and change history.
  • Assist in overall safety systems operational support for internal teams and external clients.

Reporting & Data Management

  • Develop and generate:
    • Standard safety system reports
    • Ad hoc operational reports
    • Regulatory data extracts
    • Safety listings for compliance reporting
  • Conduct routine and ad hoc data extraction for:
    • PSURs (Periodic Safety Update Reports)
    • DSURs (Development Safety Update Reports)
    • 6-month safety listings
  • Support data quality checks and reporting accuracy.

Migration, Validation & Support

  • Participate in data migration projects, migration validation, and migration documentation activities.
  • Support system change management initiatives and implementation updates.
  • Perform User Acceptance Testing (UAT) and complete required documentation.
  • Monitor support mailboxes and system queues for incident management.
  • Support ticket management, troubleshooting, and issue escalation.
  • Resolve system failures and technical incidents within expected timelines.

Training & Stakeholder Support

  • Support and educate internal users, sponsors, and operational teams on safety system usage.
  • Train team members on technical and functional aspects of pharmacovigilance platforms.
  • Respond to support mailbox queries and user requests.
  • Maintain strong collaboration across safety operations and technology teams.

Compliance & Quality

  • Complete all assignments in compliance with:
    • SOPs
    • Quality standards
    • Internal procedures
    • Current pharmacovigilance regulations
  • Maintain awareness of evolving global drug safety regulations and system compliance requirements.

Required Qualifications

  • Bachelor’s degree in:
    • Life Sciences
    • Information Technology
    • Computer Science
    • Related scientific or technical disciplines
  • Equivalent relevant experience may be considered

Experience Requirements

  • Minimum 2+ years of experience in pharmacovigilance systems, safety technology support, or drug safety platform operations
  • Hands-on experience with at least one of the following:
    • Oracle Argus Safety
    • ARISg
    • Veeva Safety
    • Equivalent drug safety platforms
  • Experience in system operations support roles preferred
  • Experience with validated document management systems desirable
  • Freshers are not eligible

Required Skills