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    Assoc Medical Data Review Mgr

    Iqvia
    3-5 years
    Preffered by Company
    Bangalore
    10 Sept. 3, 2024
    Job Description
    Job Type: Full Time Education: B.Pharm/ M.Pharm/ B.Sc/ M.Sc/ Any LifeScience 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

    Position: Medical Data Review Specialist

    Job Overview:

    As a Medical Data Review Specialist, you will provide expert medical review and project management support to ensure high-quality data management products that meet customer needs. Your role will involve comprehensive patient data review from a clinical perspective and managing structured data to ensure accuracy and compliance.

    Key Responsibilities:

    • Data Review and Analysis:

      • Identify anomalies in patient data to ensure medical congruency and adherence to protocol.
      • Conduct structured patient data reviews with minimal guidance, ensuring that data aligns with clinical expectations and standards.

    • Project Management:

      • Provide project management support by working with clinical study teams, key decision-makers, and internal members to drive continuous process improvements and manage issue escalation.
      • Track service performance and lead efforts to identify root causes of issues, implementing corrective actions as needed.

    • Customer and Team Interaction:

      • Maintain strong relationships with customers, ensuring their needs are met and addressing any issues promptly.
      • Serve as a Subject Matter Expert (SME) and provide therapeutic area or indication training to the clinical team.
      • Attend Kick-Off meetings, weekly team meetings, and client meetings as needed or requested.

    • Process Improvement and Efficiency:

      • Continuously seek opportunities to enhance task efficiency and the quality of deliverables.
      • Provide leadership in resolving compliance issues and improving overall project performance.

    Qualifications:

    • Educational Background:

      • Bachelor’s Degree in Clinical, Biological Sciences, or a related field with at least 3 years of experience in clinical practice or clinical research. An MBBS or equivalent medical degree is required.

    • Experience:

      • Proven experience in clinical data sciences within a CRO, pharmaceutical company, or similar medical environment, demonstrating leadership and project management capabilities.
      • Strong understanding of clinical/medical data and experience with medical terminology, pharmacology, anatomy, and physiology.

    • Skills and Competencies:

      • Excellent communication, interpersonal, and customer service skills.
      • Strong organizational, problem-solving, and project management abilities.
      • Ability to work independently with minimal supervision and manage multiple projects with competing priorities.
      • Proven ability to establish and maintain effective working relationships with colleagues, managers, and clients.

    About IQVIA:

    IQVIA is a leading global provider of advanced analytics, technology solutions, and clinical research services to the life sciences industry. Our mission is to push the boundaries of human and data science to create a healthier world. For more information about our career opportunities, visit IQVIA Careers.

    Apply Now

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