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Assoc Medical Data Review Mgr

2+ years
Not Disclosed
10 Dec. 26, 2024
Job Description
Job Type: Full Time Education: MBBS/MD 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 Review Specialist
Location: IQVIA Laboratories


About IQVIA:
IQVIA is a global leader in providing clinical research services, commercial insights, and healthcare intelligence to the life sciences and healthcare industries. We drive the development and commercialization of medical treatments that improve patient outcomes and population health. To learn more, visit IQVIA Careers.


Role Overview:
As a Medical Review Specialist, you will provide expert medical review and project management support to ensure that patient data is accurate and aligns with clinical study protocols. You will collaborate with clinical study teams, key stakeholders, and internal members to enhance efficiency and address issues promptly.


Key Responsibilities:

  • Patient Data Review & Quality Assurance:

    • Identify patient anomalies to ensure data congruency and plausibility as per the study protocol.
    • Ensure the medical accuracy of the data and address any discrepancies.
  • Project Management Support:

    • Provide project management expertise with minimal guidance by collaborating with clinical study teams and key decision makers.
    • Manage continuous process improvements, issue escalation, and workload projections.
    • Track service performance and identify root causes for issues, implementing corrective actions as needed.
  • Client Relationship Management:

    • Maintain strong relationships with customers and act as a Subject Matter Expert (SME).
    • Provide timely follow-up and resolution of compliance issues to ensure customer satisfaction.
  • Training & Communication:

    • Provide therapeutic area/indication-specific training for the clinical project teams.
    • Participate in Kick-Off meetings, weekly team meetings, and client meetings as required.
  • Efficiency & Deliverable Quality:

    • Continuously seek opportunities to improve task efficiency and enhance the quality of deliverables.

Qualifications:

  • Education:

    • Medical degree (MBBS or MD). Freshers with an MD or 2+ years of experience are encouraged to apply.
  • Experience:

    • 2+ years in clinical data sciences, preferably within a CRO, pharmaceutical company, or related medical environment.
    • Leadership experience and understanding of clinical/medical data.
  • Skills:

    • Strong knowledge of Medical Terminology, Pharmacology, Anatomy, and Physiology.
    • Operational focus with a clear understanding of metrics, project status, and timely issue resolution.
    • Excellent communication, interpersonal, and customer service skills.
    • Strong organizational, problem-solving, and project management skills.
    • Ability to handle multiple projects and competing priorities.

What We Offer:

  • Opportunities for professional growth in clinical research and data management.
  • Competitive compensation and benefits packages.
  • The chance to contribute to the development of impactful healthcare solutions.

Equal Opportunity Employment:
IQVIA is an equal opportunity employer, committed to fostering a diverse and inclusive workforce. We provide equal employment opportunities for all, including veterans and candidates with disabilities.

For more information, visit IQVIA Equal Opportunity.


COVID-19 Vaccination Requirement:
IQVIA may require employees to meet specific COVID-19 vaccination status requirements. For more details, visit COVID-19 Vaccine Status.