Operations Analyst I (DCR)

DaVita Kidney Care

2d • $57,784 - $76,000 • Hybrid

About The Position

At DaVita Clinical Research, we find that our best leaders are those who create an inspiring vision, have a desire to shape the future of medicine, and empower their team to achieve success. They enjoy tackling difficult problems and believe that the best way to solve them is through a collaborative environment that involves team efforts. They take ownership of results and instill accountability in those they lead. They are driven, compassionate, strong communicators, relationship builders, and find real fulfillment in challenging and impactful work. Sound like you? Then you might be a great fit for our Operations Analyst I position with DaVita Clinical Research (DCR). We are looking for a highly committed individual who will provide support to the DCR operations team as it pertains to the utilization of systems/applications in the analysis of clinical research data and quality controls. This position reports to the Operations Innovations Manager. This position is hybrid position based in Edina, MN.

Requirements

• 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
• Strong organizational skills and attention to detail​​ required.
• Travel required, less than 10%

Nice To Haves

• 3 or more years of experience with Tableau, research databases (i.e. RAVE, Medidata), Clinical Trial Management Systems preferred
• 2 years experience managing multiple projects, meeting deadlines, and adjusting priorities appropriately in an evolving work environment with shifting time frames is preferred

Responsibilities

• Follows quality control processes and can translate those process points to questions, actions and follow-up
• Reviews and compares Sponsor EDC/ IVRS data and verifies within Clinical Trial Management System (CTMS)
• Reviews and responds to CTMS data quality requests and incidents from internal and external users
• Maintains systems/ applications by researching and resolving problems; maintaining system integrity and security
• Uses internal/external applications to conduct, review and report on data quality control checks
• Provides reference for team by writing clear documentation; providing support and help
• Contribute as a team member on special projects as needed
• Attend team meetings, phone conferences, and training as needed
• Know, understand, and follow teammate guidelines, employment policies, and department or company procedures
• Ability to communicate clearly and effectively on the phone and in email
• Lead or assist with special projects and duties as assigned

Benefits

• Flexible weekly work schedule
• December Industry wellness break (Week between Christmas and New Year’s Day)
• Comprehensive benefits: Medical, dental, vision, 401(k) match, paid time off, PTO cash out
• Support for you and your family: Family resources, EAP counseling sessions, Headspace®, backup child and elder care, maternity/paternity leave
• Professional development programs
• On-demand virtual leadership and development courses through DaVita’s online training platform StarLearning
• Performance-based rewards
• Competitive total rewards package

What This Job Offers

• Job Type: Full-time
• Career Level: Entry Level