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Medical Reviewer Case Processing (Manager)

3+ years
Not Disclosed
10 May 22, 2025
Job Description
Job Type: Full Time Education: MD/DO 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

Job Title: Medical Reviewer Case Processing (Manager)
Category: Consulting
Location: Noida, India
Job Type: Full Time
Posted Date: May 20, 2025
Job ID: R257963


About Cencora:

At Cencora, our purpose is to create healthier futures. We are united in this mission, and every individual here is vital to our success. If you’re looking to make a meaningful impact in the healthcare sector, we invite you to join our passionate and innovative team.


Job Description:

As a Medical Reviewer - Case Processing (Manager level), you will be responsible for medical review, assessment, and quality oversight of ICSRs. This role involves interpreting clinical and safety data to ensure regulatory compliance and patient safety. You will also contribute to literature surveillance, signal detection, and mentoring junior PV professionals.


Key Responsibilities:

  • Conduct medical review and assessment of Individual Case Safety Reports (ICSRs)

  • Review adverse event selection, seriousness criteria, MedDRA coding, drug data, causality, narratives, and provide Company Clinical Comment

  • Respond to case owner queries within the patient safety database

  • Screen scientific literature using internal/external sources for relevant safety publications

  • Ensure compliance with GPVP, GCP, ICH, and EMA guidelines

  • Mentor PV associates in event capturing and safety conventions

  • Maintain up-to-date knowledge of product safety profiles and therapeutic areas

  • Escalate complex safety issues to Team Lead/Line Manager

  • Participate in signal detection processes and support literature classification

  • Collaborate in the preparation of PSURs, PBRERs, and RMPs

  • Take part in internal/external audits and inspections

  • Contribute to other pharmacovigilance and drug safety tasks as assigned


Qualifications & Experience:

  • Medical degree (MBBS/MD); PG qualification is preferred but not mandatory

  • Minimum 3 years of relevant experience in Pharmacovigilance and Drug Safety

  • Strong understanding of global safety databases, regulatory guidelines, and SOPs

  • Excellent interpersonal and organizational skills

  • Ability to work under pressure with a high sense of responsibility and dedication

  • Fluent in spoken and written English

  • Prior experience in corporate, pharma, or life sciences environments is an advantage


What Cencora Offers:

  • Benefits in line with local market standards (may vary by region)

  • Inclusive and respectful workplace

  • Commitment to equal employment opportunities and non-discrimination

  • Reasonable accommodations available during the hiring process for qualified individuals with disabilities


Affiliated Company: PharmaLex India Private Limited
📧 For accommodations:
hrsc@cencora.com
📞 Or call: 888.692.2272
🖥️ Visit:
www.cencora.com