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Medical Review Senior Associate Scientist

1-9 years
Not Disclosed
10 Feb. 6, 2025
Job Description
Job Type: Full Time Education: B.Sc./M.Sc./B.Pharm/M.Pharm/Life science 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 Review Senior Associate Scientist

📍 Location: Hyderabad, India
💼 Job ID: R-205815
🕒 Date Posted: Feb. 04, 2025
🏢 Work Location Type: On Site

Company Overview:

Amgen is a global biotechnology leader dedicated to serving patients with serious illnesses. With a focus on Oncology, Inflammation, General Medicine, and Rare Diseases, Amgen has made significant advancements in biotech since 1980. The company reaches millions of patients each year with innovative medicines, fostering a collaborative and science-based culture that thrives on challenges and opportunities.

Job Overview:

As a Medical Review Senior Associate Scientist at Amgen, you will provide medical review of individual safety case reports (ICSR) to support the safety surveillance of Amgen products. You will ensure the medical validity of these reports, ensuring regulatory compliance, and collaborate with the Medical Safety Review Team (MSRT).

Key Responsibilities:

  • Support global regulatory reporting compliance of individual case safety reports (ICSR).
  • Ensure the medical validity of ICSRs, including reviewing narratives, coding, expectedness, causality, and seriousness.
  • Act as a point of contact for Case Management regarding the medical content of ICSRs.
  • Perform ICSR case escalations as necessary.
  • Conduct case follow-ups per SOPs.
  • Support the medical coding conventions and process improvements in ICSR review.
  • Assess the reportability of medical device-associated or product complaint-associated events.
  • Participate in interdepartmental initiatives, including process improvement and SOP creation for medical review.
  • Maintain inspection readiness and represent the team during Health Authority inspections and internal audits.

Qualifications:

  • Basic Qualifications:
    • Master’s degree with 1 to 3 years of relevant experience, or
    • Bachelor’s degree with 3 to 5 years of relevant experience, or
    • Diploma with 7 to 9 years of relevant experience.
  • Preferred Qualifications:
    • Knowledge of Amgen’s medical review and case management SOPs.
    • Clinical knowledge of therapeutic area patient populations and drug classes.
    • Proficiency in technical safety systems, safety databases, and medical coding.
    • Experience in safety data capture in clinical trials and post-marketing settings.
    • Familiarity with Amgen’s products and patient populations.

What You Can Expect From Us:

At Amgen, you’ll enjoy competitive benefits, a collaborative culture, and a focus on your professional and personal growth. Amgen’s Total Rewards Plans are aligned with local industry standards, offering comprehensive rewards alongside a fulfilling career path.

Equal Opportunity Employer:

Amgen is an Equal Opportunity employer, committed to fostering an inclusive environment. We ensure that individuals with disabilities are provided reasonable accommodation throughout the recruitment and employment process.