***This position is contingent upon external funds***
The Study Coordinator is responsible for coordinating studies including IRB submission and maintenance of regulatory documents, enrollment of patients on assigned studies, tracking patent progress through study, data entry and other data management.
Education: High school diploma or GED, Bachelors Degree preferred.
Experience: Previous research experience required.
Skills & Abilities: Able to interact with others in a courteous, professional manner with a high level of confidentiality. Must have working knowledge of computers, preferably Microsoft Word, Microsoft Access, Microsoft Powerpoint and Microsoft Excel experience. SQL experience helpful. Excellent verbal and written communication. Strong organizational skills with the ability to analyze information and make accurate decisions. Attention to detail is required. Must be a self-starter with the ability to work with little or no supervision. Ability to work in fast paced environment and multi-task different job functions. Ability to effectively handle non-routine tasks or problems.
Sit: Up to 8 hours/day
Stand/Walk: 3-6 hours
Bend/Stoop: Up to 3 hours
Reach: Up to 3 hours
Rep Use of UE/Grasp: Up to 8 hrs
Lift/Push/Pull: 15 to 25 lbs
This job requires the ability to hear alarms clients and/or instruction. The ability to see accurately from 20 inches to 20-ft. Reasonable accommodations may be made to enable individuals with disabilities to perform the essential function of this position.