Dialysis Clinic, Inc. · 4 days ago
Clinical Research Coordinator
Dialysis Clinic, Inc. is a nonprofit organization dedicated to providing individualized care for patients with chronic kidney disease. The Clinical Research Coordinator role involves supporting and coordinating clinical trials, ensuring compliance with study protocols, and maintaining relationships with study participants and investigators.
Health CareMedicalNon Profit
Responsibilities
Ensure compliance with the clinical trial protocol and overall objectives of the study including the collection, preparation, maintenance, and submission of numerous study documents: Institutional Review Board (IRB) applications, CV's, medical licenses, case report form(s), regulatory documents binder, electronic data capture, etc.) as applicable
Perform detailed medical chart review and patient interview to ensure patient qualifies to be enrolled in the study
Manage informed consent process and ensure confidentiality practices are consistent with regulatory and study guidelines
Meet enrollment goals as directed by DCICR Director
Maintain a strong relationship with subjects involved in clinical trials and ensure that their rights as subjects are protected
Coordinate and perform study visits/procedures (vital signs, EKG's, BIA, medical history, lab procedures, etc.) per qualification and per protocol
Log and inform Principal Investigator (PI) of any possible adverse reactions or serious adverse events in a timely manner
Maintain study logs, IRB forms and Regulatory Binders for each clinical trial
Maintain a strong relationship with and be available to investigators and research, dialysis, and practice staff to ensure subject safety and compliance with the clinical trial protocol
Participate in routine monitoring visits from Sponsor and/or FDA audits
Conduct clinical trials in 2 or more outpatient dialysis units as needed
Coordinate multiple trials
Work flexible hours in order to accommodate study visits and perform job functions as needed
Travel overnight for Investigator Meetings as required
Work independently with limited supervision
Maintain and follow up with all research documentation and data involved in coordinating a clinical trial and/or multiple clinical trials in a timely manner to provide quality data and/or information
Other responsibilities as defined by DCICR Director and/or DCICR Clinical Manager
Qualification
Required
Excellent communication skills
Demonstrated clinical excellence
Desire to collaborate with care teams
Ability to problem solve
An individual with at least 2 years of experience conducting clinical trials or an individual currently employed in the medical field; dialysis experience preferred
Reliable transportation, a valid driver's license, auto insurance, and be willing to travel to multiple DCI clinics within a given territory
Benefits
Comprehensive medical, dental and vision benefits
Life and long-term care insurance provided at no additional expense to employee
Paid time off (PTO) including holidays
Extended Sick Bank (ESB) in addition to PTO – paid time for doctor appointments, sickness or medical leave
Retirement plans with $.50 of each contributed dollar matched for eligible employees, up to 8 percent
Education reimbursement
Employee assistance program
Wellness program
Among others
Company
Dialysis Clinic, Inc.
The nation's largest not-for-profit dialysis provider operating under the mission, "The care of the patient is our reason for existence." The primary responsibility of DCI is to perceive, initiate, and provide comprehensive patient care.