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Pharmacovigilance Specialist, Submissions

2+ years
Not Disclosed
10 Oct. 22, 2024
Job Description
Job Type: Full Time 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, Research & Development, Technical Skill, Triage of ICSRs, WHO DD Coding

Pharmacovigilance Specialist, Submissions

Location: Remote

About ProPharma

For the past 20 years, ProPharma has been dedicated to improving patient health and wellness by providing expert guidance to biotech, medical device, and pharmaceutical organizations. As the world's largest Research Consulting Organization (RCO), we partner with clients through an advise-build-operate model across the entire product lifecycle. Our expertise spans regulatory sciences, clinical research, quality and compliance, pharmacovigilance, medical information, and R&D technology, offering fully customizable consulting solutions to accelerate drug and device programs.

Position Overview

The Pharmacovigilance (PV) Specialist, Submissions is responsible for ensuring adherence to operational processes while managing adverse event submissions using the multi-tenant Argus and ARISg databases. This role focuses on daily tracking of adverse event reports, maintaining compliance with health authorities, ethics committees, and safety partners, and supporting submission processes for new territories and product types.

Key Responsibilities

Adverse Event Submission and Compliance:

  • Follow ProPharma processes for pharmacovigilance regulatory reporting, including monitoring expedited and non-expedited ICSR submissions.

  • Execute monthly ICSR reconciliation reports with clients and safety partners.

  • Assist in testing submissions to health authorities and exchanges with safety partners.

  • Manage submissions-related deviations and CAPAs.

Periodic Reports:

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

  • Assist in the generation and verification of custom reports for periodic reporting.

  • Support the pharmacovigilance management team in maintaining reporting services.

Submission Projects:

  • Participate in performance qualification testing for Argus upgrades and custom projects.

  • Update documentation for new territory-specific E2B profiles.

  • Test data migration imports involving the multi-tenant Argus database.

Experience Required

  • Post-secondary education or equivalent professional experience (life science degree preferred).

  • Fluent in English.

  • Proven experience in a similar role is highly preferred.

  • Proficient in Microsoft Office Suite (Outlook, Word, Excel) and strong keyboarding skills.

  • Excellent attention to detail and strong communication skills.

  • Flexibility to adapt to changing business priorities.

  • Ability to work independently and collaboratively in a multidisciplinary team.

Commitment to Diversity

At ProPharma, we celebrate our differences and strive to create a workplace where everyone can be their authentic selves. We are committed to diversity, equity, and inclusion, providing a safe space where all employees feel empowered to succeed.