Operations Analyst I (DCR)
$57,784–$76,000 year
Hybrid · Edina, Minnesota, United States
Job Summary
Operations Analyst I will support the DaVita Clinical Research (DCR) operations team by analyzing clinical research data and performing quality control across CTMS, EDC, and IVRS systems. Responsibilities include translating quality control points into actionable questions and follow-up, reviewing Sponsor EDC/IVRS data, responding to CTMS data quality requests, maintaining system integrity and security, conducting data quality checks, documenting processes, and contributing to special projects. Requires strong analytical skills, experience with Tableau and clinical trial systems, ability to manage multiple projects, and effective communication; hybrid, based in Edina, MN.
Required Qualifications
- High School Diploma or equivalent is required
- Bachelor's Degree in Statistics or related field is required
- Minimum 3 years experience performing quality control and/or compliance monitoring required
- Minimum 3 years experience translating monitoring data into executive summary level business metrics required
- Minimum 1 year experience working with Tableau, research databases (i.e. RAVE, Medidata), Clinical Trial Management Systems required; 3 or more years of experience preferred
- Minimum 2 years experience managing multiple projects, meeting deadlines, and adjusting priorities appropriately in an evolving work environment with shifting time frames is preferred
- Proven self-starter with high degree of initiative, urgency, and follow through
- Must be detail oriented with strong analytical, organizational critical thinking and communication skills
- Travel required, less than 10%
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