Clinical Research Coordinator 1

 Manages the day-to-day responsibilities of clinical research trials assigned by Director of Clinical Research. Works with both the medical community and pharmaceutical sponsors / monitors to ensure the proper conduct of studies.  

1. Program Management
   1. Independently manages the overall planning, scheduling, budgeting and monitoring of individual clinical research projects from initiation to project closeout.
   2. Coordinators subject recruitment, enrollment and study data collection.
   3. Audits and monitors patient accounts for charges specific to clinical research clients. Works with Director Clinical Research to ensure billing compliance to all third-party payors.
   4. Provide subject care and monitors for adverse events in adherence with the study protocol and in accordance with good clinical research principals.
   5. Maintains subject research charts and regulatory books for employed physicians serving as principal investigators.
2. Job Quality
   1. Utilizes all equipment, supplies facilities and resources in a prudent and efficient manner in order to ensure efficient departmental operations and the provision of high-quality health care services.
   2. Promotes the quality and efficiency of his/her own performance by remaining current with the latest trends in field of expertise through participation in job-relevant seminars and workshops, attendance at professional at conferences and affiliations with national and state professional organizations.
3. Collaboration and Partnership
   1. Manages relationships with study sponsors, investigators and associated staff to provide the highest level of customer service.
   2. Develops the clinical research department by marketing the services of the department to physicians' conduction research within OLOL and in the private practice setting.
   3. Educates hospital clinical staff, particularly Nursing Services, Pharmacy and Laboratory on clinical research studies.
   4. Maintains communication with administrative staff for pertinent research opportunities that may become problematic for OLOL structures (standards, ERDs, policies and procedures, etc.).
4. Other Duties as Assigned
   1. Performs other duties as assigned or requested.

Education - Bachelor’s Degree in Healthcare or related field OR 5 years professional-level experience