Clinical Research Coordinator (DCR)

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.

About the role

We are looking for a highly motivated, positive, and innovative Clinical Research Study Coordinator (Research Coordinator) to lead in the coordination, management, and conduct of nephrology clinical research trials in dialysis centers and physicians' practices. This position will be based in our Edina, MN site and coordinate and execute all aspects of late-phase clinical trials in the Minneapolis/St. Paul and surrounding areas. Based on business needs, a flexible weekly work schedule may be available.

Responsibilities

• Accountable for the successful execution of clinical trials through all phases of the study: enrollment, maintenance, and close out.
• Responsible for performing research procedures according to the study protocol and working in partnership with the physician investigator to coordinate research activities.
• Serves as a liaison between the physicians (Principal Investigator or Sub-Investigator), study sponsors, and DaVita facility teammates.
• Responsible for delivering or exceeding project enrollment targets for clinical research studies at their site.
• Responsible for accurate and timely data entry into the electronic data entry systems.
• Responsible for timely resolution of all data queries to meet project timelines for database lock.
• Demonstrates compliance with good clinical practice (GCP) and applicable law, and verifies that study teams comply with GCP and applicable law.
• Demonstrates adherence to DCR standard operating procedures and policies and with the standards customary in the clinical research industry.
• Understands and promotes compliance with all applicable healthcare and research regulations.

Requirements

• High School Diploma or equivalent is required.
• Bachelor's Degree is preferred.
• Minimum 1 year of clinical research experience managing studies from start-up to close out or equivalent experience.
• Reliable transportation to travel between local research sites.
• Commitment to and role model of DaVita’s values with the ability to demonstrate those positively and proactively to patients, teammates, management, physicians, and/or vendors in everyday performance and interactions.
• Ability to manage multiple projects, meet deadlines, and adjust priorities appropriately in an evolving work environment with shifting time frames; self-starter with a high degree of initiative, urgency, and follow-through.
• Experience in managing confidential information and/or issues using discretion and judgment.
• Certified Clinical Research Coordinator (SOCRA or ACRP) - preferred.

Benefits

• Flexible weekly work schedule: This will vary and is based on current business needs.
• 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, access Headspace®, backup child and elder care, maternity/paternity leave, and more.
• Professional development programs: DaVita offers a variety of programs to help strong performers grow within their career and also offers on-demand virtual leadership and development courses through DaVita’s online training platform StarLearning.

Pay

The salary range for this role is $50,000.00 - $76,000.00 per year. Compensation will depend on a number of factors, including a candidate’s qualifications, skills, competencies, and experience.