Senior Data Management Analyst - Clinical Research (Remote)

University of Kentucky

Lexington (KY)

Remote

USD 90,000 - 115,000

Full time

31 hours ago
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Benefits offered by this job

Flexible Remote Work Options
Professional Development Opportunities
Forbes recognition as top employer

Job summary

University of Kentucky is seeking a Data Management Analyst Senior (Clinical Research Associate Senior) to support and enable groundbreaking clinical research. The role offers flexible remote options and collaboration with cross-functional UK teams.

The position focuses on managing CTMS content, data entry, and calendar production to ensure accurate participant tracking and compliant billing. Strong MS Office and regulatory knowledge are preferred.

Qualifications

  • Experience with clinical research, clinical trial management systems, billing for clinical research, regulatory and financial administration.
  • Clinical research knowledge and documentation skills are preferred.

Responsibilities

  • Assist clinical research teams with CRSO services including the development of the electronic schedule of events and initial data entry content.
  • Review and interpret complex clinical research protocols to determine data entry levels in CTMS.
  • Produce clinical research calendars to drive participant tracking, compliant billing, and financial practices in CTMS and Epic billing.
  • Support CRSO as the primary contact for new studies, serving as a subject matter expert for CTMS content and minimum data requirements.

Skills

Attention to detail
Data entry accuracy
Communication skills

Tools

CTMS
Epic

Job description

University of Kentucky is seeking a Data Management Analyst Senior (Clinical Research Associate Senior) to support and enable groundbreaking clinical research. The role offers flexible remote options and collaboration with cross-functional UK teams.

The position focuses on managing CTMS content, data entry, and calendar production to ensure accurate participant tracking and compliant billing. Strong MS Office and regulatory knowledge are preferred.

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