The Advisor Clinical Research plays a key role in developing two main artefacts Human Readable and Data Dictionary using MAT tool and analyze measure specifications to translate data in clinical form. This role works closely with clinical teams, database management personnel, and project managers.
Job Responsibilities:
Registry Data Management:
- Create two main artefacts: Humar Readable and Data Dictionary.
- Maintaining the artefacts for every performance year.
- Analyzing 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.
Required Qualifications:- Bachelor's or Master's 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
Work Experience:
