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Pspm Support Associate

Fortrea
1-2 years
INR 4 LPA – 6 LPA
Bangalore, India
1 June 17, 2026
Job Description
Job Type: Full Time Education: B.Sc/M.Sc/M.Pharma/B.Pharma/Life Sciences Skills: GCP guidelines, HCPCS Level II, ICD-10-CM, ICD-10 CM Codes, CPT-Codes, HCPCS Codes, ICD-10 CM, CPT, HCPCS Coding

PSPM Support Associate

Location: Bangalore
Employment Type: Full Time


Job Overview

The PSPM Support Associate is responsible for supporting Clinical Safety and Pharmacovigilance Services (PSS) operations associated with clinical trials and post-marketing products. The role involves assisting with safety project management activities, adverse event reporting processes, safety documentation, study start-up activities, safety database reconciliation, and compliance with global regulatory requirements.

The position supports Global Safety Leads and project teams in delivering high-quality pharmacovigilance services while ensuring compliance with client requirements, SOPs, and international safety reporting regulations.


Summary of Responsibilities

Project Support & Safety Operations

  • Support the setup, maintenance, and close-out of global and regional clinical trial and post-marketing safety projects.

  • Assist Global Safety Leads in managing project-specific safety activities.

  • Support study start-up activities and ongoing project maintenance.

  • Assist with project functional management activities, including:

    • User access requests

    • Training assignments

    • Project tracking activities

  • Support system setup and maintenance activities throughout the project lifecycle.

Safety Documentation & Compliance

  • Assist in the preparation of:

    • Safety Management Plans (SMPs)

    • Reconciliation Plans

    • Safety-specific project plans

    • Study-specific job aids

    • Training materials

    • Templates and instructions

  • Ensure compliance with:

    • Company SOPs

    • Client requirements

    • Global Pharmacovigilance regulations

    • Safety processing guidelines

Safety Reporting & Reconciliation

  • Support reconciliation activities between safety databases and other study systems.

  • Assist in ensuring accurate and timely safety reporting.

  • Support adverse event management and safety case processing activities.

  • Contribute to maintaining data quality and reporting compliance.

Project Reporting & Communication

  • Assist Global Safety Leads in generating:

    • Monthly status reports

    • Project-specific reports

    • Safety metrics and dashboards

  • Verify quality and accuracy of project data and metrics.

  • Support preparation of safety presentations for internal and external stakeholders.

  • Assist in communication and coordination across project teams.

TMF & Audit Support

  • Support Trial Master File (TMF) management activities.

  • Assist in preparing safety documentation for:

    • Internal audits

    • Client audits

    • Regulatory inspections

  • Ensure documentation is inspection-ready and compliant.

Process & Quality Compliance

  • Maintain knowledge of applicable SOPs and controlled documents.

  • Demonstrate compliance with company quality standards and safety procedures.

  • Ensure accurate and timely completion of assigned deliverables.

  • Support continuous improvement initiatives where required.

  • Perform additional duties as assigned.


Qualifications (Minimum Required)

Any of the following combinations are acceptable:

  • Non-degree qualification with:

    • 1 year of Safety experience, or

    • 3 years of relevant industry experience

  • Associate Degree with:

    • 1 year of Safety experience, or

    • 2 years of relevant experience

  • Bachelor's Degree (BS/BA) with:

    • 1 year of relevant experience

  • Master's Degree (MS/MA) with:

    • 1 year of relevant experience

  • PharmD with:

    • 1 year of relevant experience

    • A one-year residency or fellowship may be considered equivalent experience

Preferred Educational Background

  • Biological Sciences

  • Pharmacy

  • Nursing

  • Medical Sciences

  • Life Sciences

  • Healthcare or Related Scientific Disciplines


Experience (Minimum Required)

  • Experience in:

    • Pharmacovigilance

    • Clinical Safety

    • Drug Safety Operations

    • Clinical Research

    • Healthcare Support Functions

  • Strong attention to detail and accuracy.

  • Ability to work independently with moderate supervision.

  • Strong organizational and multitasking abilities.

  • Team-oriented approach with willingness to support colleagues.

  • Good written and verbal communication skills.

  • Strong documentation and administrative skills.

  • Knowledge of:

    • Microsoft Office Suite

    • Windows Operating Systems

    • Safety Databases (preferred)


Preferred Skills

  • Clinical Trial Safety Management.

  • Pharmacovigilance Operations.

  • Safety Project Coordination.

  • Safety Reporting and Compliance.

  • TMF Management.

  • Safety Database Reconciliation.

  • Regulatory Documentation Support.

  • Audit and Inspection Readiness.