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Pharmacovigilance Specialist, Submissions

Propharma
Propharma
0-2 years
Not Disclosed
Remote, India, India
10 May 6, 2026
Job Description
Job Type: Full Time Remote Education: B.Sc./ M.Sc./ M.Pharm/ B.Pharm/ Life Sciences 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

Company Overview

ProPharma Group has over 20 years of experience improving patient health and wellness by supporting biotech, medical device, and pharmaceutical organizations.

Through its advise–build–operate model, ProPharma delivers end-to-end solutions across the product lifecycle, with expertise in:

  • Regulatory Sciences

  • Clinical Research Solutions

  • Quality & Compliance

  • Pharmacovigilance

  • Medical Information

  • R&D Technology


Role Title

Pharmacovigilance (PV) Specialist – Submissions


Role Summary

The PV Specialist – Submissions is responsible for ensuring compliance with adverse event reporting requirements by working within a multi-tenant Argus database.

The role focuses on:

  • Tracking adverse event submissions

  • Ensuring regulatory compliance with global health authorities

  • Supporting system testing and submission processes

  • Maintaining submission and exchange compliance with safety partners


Key Responsibilities

1. Adverse Event Submission & Compliance

  • Follow ProPharma pharmacovigilance processes and regulatory reporting guidelines

  • Monitor daily:

    • Expedited and non-expedited Individual Case Safety Reports (ICSRs)

    • Submission schedules and exchanges

  • Perform monthly ICSR reconciliation with clients and safety partners

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

  • Assist in managing submission-related deviations and CAPAs


2. Periodic Reports

  • Generate Argus-based:

    • Line listings

    • Summary tabulations

  • Support creation and verification of custom reports

  • Assist in setup and validation of periodic reporting requirements

  • Coordinate with PV management on reporting activities


3. Submission Projects & System Testing

  • Perform tester role in:

    • Performance Qualification (PQ) testing for Argus upgrades and patches

    • Custom system projects

  • Support:

    • New territory-specific E2B profile setup

    • Custom E2B profile implementation

  • Conduct PQ testing for:

    • Data migration imports into Argus database

  • Update processes and documentation as required


Education Requirements

  • Post-secondary education (Life Sciences preferred)

  • Equivalent professional experience may be considered


Experience Requirements

  • Prior experience in a similar pharmacovigilance or submissions role preferred

  • Familiarity with safety databases (e.g., Argus) is an advantage


Skills & Competencies

  • Fluency in English

  • Strong attention to detail

  • Excellent verbal and written communication skills

  • Good interpersonal skills

  • Proficiency in:

    • Microsoft Office (Outlook, Word, Excel)

    • General computer and data entry skills

  • Ability to:

    • Adapt to changing business priorities

    • Work independently and within a team


Work Environment

  • Remote work supported

  • Hybrid work encouraged for employees near office locations


Work Culture & Values

  • Commitment to Diversity, Equity & Inclusion

  • Equal Opportunity Employer

  • Encourages innovation, collaboration, and authenticity

  • Provides a supportive and inclusive workplace


Application Process

  • All applications are personally reviewed by the recruitment team

  • No AI-based screening tools are used

  • All candidates will receive an application outcome


Important Notice

  • ProPharma does not accept unsolicited resumes from recruiters or third parties

  • No phone calls or emails regarding this role