Monday - Friday, 8:00a - 4:30p, 80 hours per two-week pay period, East Campus.
Position Title: Clinical Research Coordinator
Department: Cardiac Services
Purpose: Responsible for coordinating all aspects of clinical research trials including protocol feasibility review, IRB application, protocol budgetary preparation, patient recruitment, enrollment, patient consents, patient scheduling, maintaining all necessary documentation, primary contact for patients and sponsors, and coordination of monitoring visits. Assists principal investigator in a leadership role in all aspects of conducting trials. Coordinates comprehensive patient protocol treatment schedules to maintain compliance to protocol requirements. May be required to work on multiple trials in various specialties. Provides reports to study sponsors, Genesis Heart Institute IRB, FDA and various oversight committees within GMC. Performs clinical research testing and monitors safety of subjects throughout the study. Assumes 24-hour accountability for study subject needs.
Report To: Executive Director, Cardiac Services
Supervisory Responsibility: No Supervision: The job does not require the provision of guidance or supervision to others. There is no formal responsibility for directing others.
Materials Responsibility: Moderate: Work requires moderate responsibility for material resources. Examples of resources could include operating budgets for a work unit or department, specialized equipment, costly or unusual materials or supplies, large amounts of cash or other material assets. The employee has a moderate amount of control over these resources. The cost of errors might result in moderate damage, waste or financial loss. The difficulty, variety and depth of problems associated with these material resources is moderately complex.
Key Relationship: Co-workers/Health System Employees, Outside Agencies/Other Health Care Providers, Governing Boards, General Public/Visitors/Volunteers, Physicians/Medical Office Staff, Students/Interns/Residents/Outside Instructors, Patients, Families, and Significant Others, Vendors/Clients, Third Party Payors/Insurance Companies, Auditors/Review Agencies.
Education: 4 year college/university degree or equivalent experience
Field Of Study: Nursing, Radiological Technology
Special Training: Basic Life Support
Training Preferred: Certified Clinical Research Coordinator (CCRC)
Licensure/Registration: Radiological Technologist Registered (RTR) or Registered Nurse in the State of Iowa
Experience: More than 5 years experience required.
Interpersonal Skills: Interaction is with a variety of people inside or outside the organization. Communications are often difficult or stressful in nature. Contact with others involves complex, detailed and often sensitive topics. The job requires a high degree of interpersonal skills to deal with a range of complicated problem situations. Interactions involve gaining the agreement of others.
Physical Demands: Moderate Intensity: Work requires moderate physical exertion. Forces exerted are equivalent to lifting between 10 and 25 pounds. Job requirements for manual dexterity or physical manipulation are also moderate. The need for physical stamina and endurance is of some significance. The degree of physical strain produced on the job is somewhat taxing, and maybe fatiguing. Work could involve a considerable amount of walking, standing, a confining or tiring work position, or periods of sitting in one position. However, freedom of movement does exist. The position exceeds these moderate intensity demands rarely, 10% of the time or less.
Working Conditions: There is very limited exposure to adverse environmental conditions. Some undesirable or unpleasant environmental characteristics may occur but the physical environment is generally safe and there is minimal health risk. No safety equipment or unusual precautions are required. The amount of time the employee may experience these minor adverse conditions would be limited to 10% or less of the work day.
Possible Exposure to Blood Borne Pathogens: Yes