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Medical Safety Writer

2+ years
Not Disclosed
10 Oct. 14, 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

Medical Safety Writer
Req # JR - 150057
Location: Ahmedabad, Gujarat, India
Job Category: GST Operations
Date Posted: 10/10/2024

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Join Us in Saving Lives

At Baxter, our mission is deeply ingrained in everything we do. Every role contributes to making a positive impact on patients worldwide, ensuring you feel a sense of purpose as your work improves health outcomes for millions.

Baxter’s products and therapies are essential in nearly every hospital, clinic, and home. For over 85 years, we have led the way in medical innovation, transforming healthcare.

We foster a collaborative environment where you can thrive and inspire others—this is where you can do your best work.

Role Overview

The Medical Safety Writer (MSW) is pivotal in preparing and completing aggregate safety reports for regulatory submission globally.

Key Responsibilities

  • Write and prepare standalone post-marketing aggregate safety reports, including:
    • Periodic Adverse Drug Experience Reports (PADERs)
    • Periodic Benefit Risk Evaluation Reports (PBRERs)
    • Periodic Safety Update Reports (PSURs)
  • Conduct quality control reviews of all aggregate safety reports.
  • Ensure timely processing and submission of reports according to regulatory requirements and internal timelines.
  • Assist in crafting timely responses to regulatory authority requests and assessment reports.
  • Collaborate with Drug Safety Physicians, EU-QPPV, and the GPS Risk Management team on safety writing activities.
  • Work with various Baxter teams, such as Regulatory Affairs and Clinical/Medical Affairs, as needed.
  • Support the creation and maintenance of standardized procedures in Medical Safety Writing.
  • Participate in assigned project teams and committees.

Reasonable Accommodations

Baxter is committed to providing reasonable accommodations to individuals with disabilities. If you require assistance during the application or interview process, please let us know your needs and contact information.

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