Analyst - Clinical Research

Role Overview: As an Analyst Clinical Research, you will play a key role in developing two main artefacts: Human Readable and Data Dictionary using MAT tool. You will analyze measure specifications to translate data into clinical form while working closely with clinical teams, database management personnel, and project managers. Key Responsibilities: - Registry Data Management: - Create two main artefacts: Human Readable and Data Dictionary. - Maintain the artefacts for every performance year. - Analyze CMS published documents for any updates. - Ensure timely and accurate submission of required registry reports. - Data Analysis & Reporting: - Analyze codes for annual updates and code cleaning activity. - Interpret clinical information into standard data format. - Generate periodic reports for clinical departments and leadership. - Compliance & Quality Assurance: - Ensure adherence to registry guidelines and CMS standards. - Protect patient confidentiality and ensure compliance with HIPAA/data privacy regulations. - Stakeholder Coordination: - Collaborate with researchers and data coordinators to improve data collection. - Provide training, guidance, and support to team members as needed. - Communicate effectively with internal teams and external registry partners. Qualification Required: - Bachelors or Masters degree in Life Sciences, Public Health, Health Informatics, Nursing, BDS, MBBS, BAMS, BHMS. - Experience in clinical data management, registry operations, or clinical research. - Strong proficiency in Excel and familiarity with data tools (SQL, R, SAS, Python, or data visualization platforms). - Knowledge of medical terminology, clinical workflows, and data standards (e.g., ICD, CPT, HCPCS, SNOMEDCT). - Understanding of HIPAA and clinical research regulatory requirements. (Note: No additional details of the company were provided in the job description.),