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Literature Review Specialist

2-3 years
Not Disclosed
10 Sept. 23, 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

Join Baxter: Where Your Work Saves Lives

At Baxter, we are united by a powerful mission. Every role within our organization contributes to a positive impact on lives around the world. You’ll experience a profound sense of purpose, knowing that your efforts improve outcomes for millions of patients.

For over 85 years, Baxter has been at the forefront of medical innovation, providing products and therapies that are essential in hospitals, clinics, and homes globally. Together, we cultivate an environment where we inspire each other, enabling you to do your best work.

About the Role

As a key member of the Safety Operations team within Global Patient Safety (GPS), you will serve as a subject matter expert in literature review and intake activities. This role involves performing thorough reviews of literature abstracts and articles, as well as the intake of literature cases.

Essential Duties and Responsibilities

  • Literature Review:
    Review weekly literature abstracts to identify valid and invalid safety cases.

  • Full Text Review:
    Order and evaluate full-text literature articles as necessary for safety case creation.

  • Case Intake:
    Process and log valid and invalid safety cases from your literature reviews.

  • Quality Control:
    Conduct quality control checks on abstract and article reviews, both in-line and retrospectively as needed.

  • Training:
    Facilitate new hire training and certification for literature review and intake processes.

  • Administrative Tasks:
    Order copyrights and translations as required, and perform follow-up activities for literature cases.

  • Additional Case Intake:
    Handle intake activities for cases from other sources as necessary.

Qualifications

  • Medical and Clinical Knowledge:
    Strong understanding of clinical practices and pharmacovigilance.

  • Communication Skills:
    Excellent oral and written communication abilities.

  • Team Collaboration:
    Effective team player with the ability to work independently under strict deadlines.

  • Multi-Tasking Ability:
    Skillful in prioritizing and managing a dynamic workload.

  • Regulatory Knowledge:
    Familiarity with worldwide and regional safety regulations.

  • Technical Proficiency:
    Proficient in the Pharmacovigilance Safety System and literature tracking tools.

  • Reading Comprehension:
    Strong analytical and reading comprehension skills.

Education and Experience

  • Degree:
    Bachelor’s degree in Nursing, Pharmacy, Science, or a related field.

  • Experience:
    2-3 years of experience in hospital or patient care settings; experience in the pharmaceutical industry (regulatory or safety) is preferred.

Reasonable Accommodations

Baxter is dedicated to providing reasonable accommodations for individuals with disabilities. If you require assistance during the application or interview process due to a medical condition or disability, please click here to let us know your needs along with your contact information.

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