Advisor- Clinical Research

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:

• 7 years plus