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Intake Specialist, Pv

3+ years
Not Disclosed
10 Dec. 18, 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

Intake Specialist, PV - Baxter

Req # JR - 148554
Location: Gurgaon, Haryana, India
Job Category: Patient Safety
Date Posted: 12/16/2024

About Baxter:

At Baxter, we are committed to saving and sustaining lives. Our mission connects us deeply, and no matter your role at Baxter, your work has a positive impact on patients worldwide. For over 85 years, Baxter has been a pioneer in healthcare innovations, making a significant difference in hospitals, clinics, and homes. Join us and become part of a team that inspires and works towards improving patient outcomes globally.

Role Overview:

As an Intake Specialist, you will be part of the Safety Operations team responsible for managing country-level Pharmacovigilance (PV) activities. This includes the collection, documentation, and processing of local adverse event (AE) reports from various sources, following national regulations and Baxter’s procedures.

Essential Duties and Responsibilities:

  • Manage collection, documentation, and processing of local AE reports in line with national legislation and Baxter’s internal procedures.
  • Perform surveillance activities to identify new potential safety information and escalate as needed.
  • Conduct local case triage, including assessment of validity, duplicate checks, and forwarding cases to internal/external partners.
  • Case intake within the Pharmacovigilance Safety System (PSS).
  • Respond to queries from the global case processing team.
  • Perform source document redaction and ensure proper documentation is captured in PSS.
  • Conduct local quality checks as required.
  • Perform Health Authority case downloads and other related activities as required.

Qualifications:

  • Strong oral and written communication skills.
  • High attention to detail and ability to work in a team environment.
  • Capable of working independently under tight deadlines and changing priorities.
  • Ability to multi-task, prioritize workloads, and adapt to daily changes.
  • Medical and clinical knowledge is required.
  • Proficiency in working with the Pharmacovigilance Safety System.

Education and Experience:

  • A degree in sciences, pharmacy, or a related field, or at least three years of pharmacovigilance experience.

Additional Information:

Baxter is an Equal Opportunity Employer, committed to providing reasonable accommodations for individuals with disabilities throughout the application and interview process.