Instagram
youtube
Facebook

Medical Data Review Mgr

5-7 years
Preffered by Company
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:

The Medical Data Review Specialist plays a critical role in delivering high-quality medical data review products that meet customer needs. As an expert in data management, this position provides project management for clinical data review and ensures end-to-end study data quality and integrity. The role includes offering medical, clinical, and scientific advisory expertise and driving improvements in efficiency and deliverables.

Key Responsibilities:

  • Data Analysis and Quality Assurance:

    • Conduct in-stream data trend analysis to ensure data quality and integrity, focusing on protocol compliance and targeted review of patient data.
    • Ensure data quality is maintained with a focus on audit readiness and compliance with Clinical Compliance and Systems Validation standards.
  • Requirements and Representation:

    • Define data capture requirements aligned with protocol and reporting needs.
    • Represent clinical data science at multi-disciplinary team meetings and external meetings.
  • Customer Relations and Leadership:

    • Maintain strong relationships with customers and provide leadership to identify root causes of issues, track service performance, and implement remedial actions.
    • Ensure timely resolution of compliance issues and continuously seek opportunities to improve efficiency and quality of deliverables.
  • Training and Meetings:

    • Provide therapeutic area and indication training for the project clinical team.
    • Attend Kick-Off meetings, weekly team meetings, and client meetings as needed or requested.
  • Staff Management:

    • Manage staff in accordance with organizational policies and regulations, including performance appraisal, professional development, and addressing employee relations issues.

Qualifications:

  • Educational Background:

    • Bachelor’s Degree in Clinical, Biological, Mathematical Sciences, or a related field, or a nursing qualification, with 7 years of relevant work experience. Alternatively, a combination of education, training, and experience in lieu of a degree.
  • Experience:

    • At least 7 years of experience in clinical data sciences within a CRO, pharmaceutical company, or similar medical environment, with demonstrated leadership experience.
    • Proven expertise in clinical and medical data management, including proactive issue identification and resolution.
  • Skills and Competencies:

    • Strong understanding of medical terminology, pharmacology, anatomy, and physiology.
    • Proven ability to plan, organize, and manage resources to achieve study or project goals in line with quality and time-based metrics.
    • Excellent organizational, problem-solving, and project management skills.
    • Ability to work independently with minimal supervision and manage multiple projects and competing priorities.
    • Strong communication, interpersonal, and customer service skills.
    • Ability to establish and maintain effective working relationships with coworkers, 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. We are committed to pushing the boundaries of human science and data science to create a healthier world. To learn more about our career opportunities, visit IQVIA Careers.

Apply Now