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Pharmacovigilance Specialist, Submissions

Propharma
1-4 years
₹5–9 LPA
Remote, India, India
15 June 19, 2026
Job Description
Job Type: Full Time, Hybrid, Remote Education: B.Sc./ M.Sc./ M.Pharm/ B.Pharm/ Life Sciences Skills: ICH guidelines, ICSR Case Processing, Labelling Assessment, MedDRA Coding, mRS and EQ-5D-5L, Triage of ICSRs, WHO DD Coding

Pharmacovigilance Specialist – Submissions

Company: ProPharma Group
Location: India (Remote / Hybrid)
Job ID: JR 8766
Employment Type: Full-Time
Department: Pharmacovigilance / Regulatory Submissions

Job Summary

The Pharmacovigilance Specialist – Submissions is responsible for ensuring compliant and timely adverse event (ICSR) submissions to health authorities, ethics committees, institutional review boards, and safety partners. The role focuses on operational oversight of PV submission systems (including Argus), regulatory compliance, periodic reporting, and system testing activities to support global pharmacovigilance operations.

Key Responsibilities

ICSR Submission & Compliance

  • Monitor daily expedited and non-expedited ICSR submissions and safety data exchanges.

  • Ensure compliance with pharmacovigilance regulatory reporting requirements.

  • Perform ICSR reconciliation with clients and safety partners on a monthly basis.

  • Track submission timelines and ensure adherence to regulatory deadlines.

Safety System Operations (Argus)

  • Work within multi-tenant Argus safety database for case processing and submissions.

  • Support configuration and validation of submission workflows.

  • Assist in maintaining system compliance for global PV operations.

Regulatory Submission Testing

  • Support gateway-to-gateway submission testing with health authorities.

  • Execute testing for E2B profile updates, new territories, and product expansions.

  • Participate in performance qualification (PQ) testing for system upgrades and patches.

  • Support data migration testing and validation activities.

Periodic Safety Reporting

  • Generate line listings and summary tabulations using Argus for Periodic Safety Reports.

  • Assist in preparation and verification of periodic safety reporting requirements.

  • Support setup of reporting templates for health authority submissions.

  • Assist in custom report generation and validation.

Quality Assurance & CAPA Management

  • Assist in identification, documentation, and closure of submission-related deviations.

  • Support CAPA (Corrective and Preventive Action) processes.

  • Ensure compliance with internal PV processes and global regulatory standards.

Cross-Functional Support

  • Collaborate with PV management teams on reporting service delivery.

  • Support process updates for new regulatory requirements and territories.

  • Contribute to continuous improvement of submission workflows and PV systems.

Required Qualifications

Education

  • Post-secondary education in Life Sciences or related discipline preferred:

    • Pharmacy

    • Life Sciences

    • Biotechnology

    • Biomedical Sciences

    • Equivalent professional experience accepted

Experience

  • Prior experience in Pharmacovigilance or regulatory submissions preferred.

  • Experience working with Argus safety database is highly desirable.

  • Exposure to:

    • ICSR submissions

    • Regulatory reporting

    • E2B transmission standards

    • PV compliance processes

Technical Skills

  • Argus Safety Database (preferred)

  • ICSR submission workflows

  • E2B regulatory messaging standards

  • Pharmacovigilance systems and processes

  • Microsoft Office Suite (Excel, Word, Outlook)

  • Data reconciliation and reporting tools

Key Skills

  • Strong attention to detail

  • Regulatory compliance understanding

  • Analytical and problem-solving ability

  • Documentation accuracy

  • Communication (written & verbal)

  • Ability to manage multiple priorities

  • Team collaboration and independent execution

Key Contribution

  • Ensure accurate and timely regulatory submission of safety data globally.

  • Maintain compliance with health authority reporting requirements.

  • Support integrity of pharmacovigilance submission systems and processes.

  • Enable efficient safety data exchange across global partners.

Salary Criteria

Expected Salary: ₹5–9 LPA for candidates with 1–4 years of Pharmacovigilance submissions, Argus safety system, or regulatory reporting experience; candidates with strong E2B gateway testing and global submission exposure may earn ₹9–11+ LPA depending on system expertise and regulatory domain depth.