Clinical Research Per Diem

What You’ll Do

• Collect and organize data and compile for progress reports
• Coordinate with research assistants/student employees, provide guidance and assistance as needed
• Affirm and coordinate with Research Manager to ensure clinical research and activities are performed in accordance with approved IRB
• Discuss study protocols with patients and verify the informed consent documentation
• Provide patient with written communication of their participation (i.e. copy of the signed informed consent)
• Adhere to Good Clinical Practices and the study protocols
• Ensure scientific integrity and accuracy of data and protect the rights, safety, and well-being of patients enrolled in clinical trials
• Prepare findings for publication and assist in laboratory analysis, quality control, or data management
• Write and contribute to publications
• Ensure that non-serious and serious adverse events are properly documented and reported
• Liaison to partnering hospitals and other research sites for new and existing patients
• Prepare and submit initial review of new studies to IRB
• Assist with overflow Medical Assistant duties
• Compliance with HIPAA and OSHA regulations

Qualifications

• Bachelor's degree in Human Health Care or related field required.
• Any combination of education, training, and experience that demonstrates the ability to perform the duties of the position.
• Experience with Electronic Medical Records
• Excellent computer skills
• EMR Systems
• Practice Management System
• Microsoft Suite (including: Outlook, Word, Excel, Calendar)
• Phone software
• Navigating Insurance Authorization websites
• Knowledge of estimated co-payment and co-insurance
• Specialties such as: Spine, Joints/Trauma, Sports Medicine, Foot/Ankle, and Hand/Microsurgery
• General understanding of processing legal forms
• Ability to collaborate with supervisory teams and administrators on projects or assigned tasks