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Clinical Report Reviewer

3-4 years
6-8 Lacs per annum
10 Jan. 23, 2025
Job Description
Job Type: Full Time Education: B.Sc,M.Sc,B.Pharma,M.Pharma,LifeScience Graduates 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: Clinical Report Reviewer
Location: Mohali/Chandigarh
Vacancy: 10

Job Overview:
We are looking for a detail-oriented Clinical Report Reviewer with expertise in reviewing clinical trial documents. The ideal candidate will be responsible for reviewing Clinical Trial Protocols (CTP), Case Report Forms (CRF), Informed Consent Forms (ICF), and Clinical Trial Reports (CTR) to ensure accuracy, compliance, and consistency with regulatory guidelines and company standards.

Key Responsibilities:

  • Review Clinical Trial Protocols (CTPs) to ensure clarity, accuracy, and adherence to regulatory standards.
  • Assess Case Report Forms (CRFs) and Informed Consent Forms (ICFs) for completeness and compliance.
  • Evaluate Clinical Trial Reports (CTRs) for scientific accuracy, consistency, and alignment with the protocol.
  • Ensure all documents meet the required regulatory and ethical standards.
  • Provide feedback and suggestions for improvements to clinical documentation.
  • Collaborate with clinical teams to resolve any discrepancies or issues identified during the review process.
  • Maintain up-to-date knowledge of regulatory requirements and industry best practices.

Qualifications:

  • 3-4 years of experience in clinical trial document review or related fields.
  • Strong understanding of clinical trial documentation including protocols, CRFs, ICFs, and CTRs.
  • Familiarity with regulatory guidelines and industry standards in clinical research.

Compensation:

  • Annual Salary: ₹6,00,000 - ₹8,00,000

Skills & Competencies:

  • Excellent attention to detail and critical thinking skills.
  • Strong understanding of clinical research processes and documentation standards.
  • Ability to effectively review and provide constructive feedback on clinical trial documents.
  • Good communication skills and ability to collaborate with cross-functional teams.
  • Proficiency in MS Office and relevant tools for document review.

How to Apply:
Interested candidates are encouraged to apply by submitting their updated resume and relevant experience details on hr@indivirtus.com with CC to admin1@indivirtus.com