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Pspm Support Associate

Fortrea
1+ years
4 LPA - 8 LPA
Bangalore, India
1 June 22, 2026
Job Description
Job Type: Full Time Education: B.Sc/M.Sc/M.Pharma/B.Pharma/Life Sciences Skills: ICH guidelines, ICSR Case Processing, Labelling Assessment, MedDRA Coding, mRS and EQ-5D-5L, Triage of ICSRs, WHO DD Coding

PSPM Support Associate

Location: Bangalore, India
Company: Fortrea
Department: Pharmacovigilance / Patient Safety & Pharmacovigilance Management (PSPM)
Employment Type: Full-Time

Role Summary

The PSPM Support Associate provides operational and administrative support for Clinical Safety and Pharmacovigilance projects across clinical trials and post-marketing programs. The role supports Global Safety Leads in study start-up, maintenance, reconciliation activities, safety documentation, reporting, audit readiness, and project coordination while ensuring compliance with global pharmacovigilance regulations and company SOPs.

This position plays a critical role in supporting safety operations, maintaining project documentation, and ensuring high-quality safety deliverables for sponsors and regulatory authorities.

Key Responsibilities

Clinical Safety Project Support

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

  • Assist Global Safety Leads with project coordination activities.

  • Support safety operations across:

    • Clinical Trials

    • Post-Marketing Surveillance Programs

    • Safety Monitoring Activities

Safety Documentation & Planning

  • Assist in preparation of:

    • Safety Management Plans (SMPs)

    • Reconciliation Plans

    • Safety-Specific Plans

    • Study-Specific Templates

    • Job Aids

    • Work Instructions

    • Training Materials

  • Ensure documentation is maintained according to company standards.

Safety Systems & Database Support

  • Support safety system setup during study start-up.

  • Assist with ongoing system maintenance activities.

  • Coordinate:

    • User Access Requests

    • Training Assignments

    • System Tracking Activities

  • Support safety database reconciliation activities.

Reporting & Metrics Management

  • Generate and support:

    • Monthly Status Reports

    • Project Metrics Reports

    • Safety Tracking Reports

  • Ensure quality, accuracy, and completeness of reported data.

  • Maintain project tracking tools and dashboards.

Safety Operations Support

  • Support adverse event and safety case management activities.

  • Assist in safety data reconciliation processes.

  • Ensure compliance with:

    • Safety Reporting Requirements

    • Internal SOPs

    • Client Procedures

    • Regulatory Requirements

  • Support safety-related operational deliverables.

Audit & Inspection Readiness

  • Assist in preparation of safety documentation for:

    • Internal Audits

    • Client Audits

    • Regulatory Inspections

  • Support audit readiness activities.

  • Maintain inspection-ready documentation.

TMF & Documentation Management

  • Support Trial Master File (TMF) activities.

  • Maintain safety-related study documentation.

  • Ensure accurate filing and document tracking.

  • Support document quality and completeness reviews.

Stakeholder & Communication Support

  • Support communication with:

    • Internal Safety Teams

    • Global Safety Leads

    • Project Teams

    • Clients

  • Assist in developing and delivering safety presentations.

  • Support project meetings and follow-up activities.

Compliance & Quality Management

  • Maintain understanding of:

    • Pharmacovigilance Regulations

    • Company SOPs

    • Controlled Documents

  • Ensure compliance with global safety reporting requirements.

  • Participate in continuous improvement initiatives.

Required Qualifications

Education

One of the Following:

  • B.Sc

  • M.Sc

  • B.Pharm

  • M.Pharm

  • Pharm.D

  • BDS

  • Nursing Degree

  • Life Sciences Degree

  • Medical Sciences Degree

Experience

  • 1+ year of Pharmacovigilance/Safety experience
    OR

  • 1–3 years of relevant Life Sciences or Clinical Research experience.

Preferred Experience

  • Pharmacovigilance Operations

  • Clinical Safety Support

  • Safety Database Management

  • TMF Management

  • Clinical Research Operations

  • Regulatory Documentation