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Pv Risk Management Specialist

0-1 years
£30,000 – £40,000 per annum
5 Dec. 2, 2025
Job Description
Job Type: Full Time Education: B.Pharm, M.Pharm, Pharm D., BSc., MSc. 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

PV Risk Management Specialist – Baxter | Reading, United Kingdom

Job ID: JR-190607
Category: Patient Safety / Pharmacovigilance
Location: Reading, England, United Kingdom
Date Posted: 10 November 2025
Experience Required: Fresher


About the Role

Baxter is seeking a PV Risk Management Specialist to join its Global Patient Safety (GPS) organization. This role supports the development, authoring, and maintenance of Pharmacovigilance Risk Management Plans (PV-RMPs) for Baxter’s drug and biologic portfolio.
It offers an opportunity for freshers with strong scientific and analytical skills to step into global pharmacovigilance and contribute to patient-centric risk management activities.

Baxter’s mission to Save and Sustain Lives guides every decision, product, and process. As part of this team, you will help ensure that safety measures, post-marketing commitments, and regulatory expectations are met across multiple global markets.


Key Responsibilities

  • Serve as the primary author for PV-RMPs using regional, local, and company templates.

  • Ensure PV-RMPs are developed in alignment with all applicable regulatory requirements.

  • Coordinate cross-functional reviews and secure internal approvals for submissions.

  • Support responses to Health Authority queries related to risk management plans.

  • Manage project timelines for preparation, review, and submission of PV-RMP documents.

  • Represent the GPS Risk Management function on multidisciplinary teams.

  • Collaborate with global and country-specific teams on PV-RMP development and associated commitments.

  • Assist in the planning, tracking, and oversight of commitments within the risk management process.


Who Can Apply (Fresher-Friendly Criteria)

  • Bachelor’s degree in Nursing, Pharmacy, Life Sciences, Biotechnology, Medicine, or any clinical/biological discipline.

  • Strong scientific writing ability and interest in global safety regulations.

  • Excellent analytical, communication, and critical-thinking skills.

  • Ability to manage timelines, coordinate with cross-functional teams, and be detail-oriented.

  • Familiarity with pharmacovigilance concepts or regulatory requirements is preferred but not mandatory for freshers.

(Note: The original employer requires 2+ years of PV experience, but this version is optimized for freshers as requested.)


What You Will Gain

  • Exposure to global pharmacovigilance operations.

  • Hands-on experience in PV-RMP creation and regulatory process management.

  • Opportunities to participate in cross-regional safety initiatives.

  • Structured professional development and learning support.


Benefits Offered by Baxter

  • Competitive compensation package.

  • Career development and long-term learning opportunities.

  • Strong work–life balance culture.

  • Pension and life assurance programs (country-specific).