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Job Title: Clinical Research Nurse
Job Number:
Organization: Inova Health System
Posted: 9/4/2017
Type: Full-Time
Number of Openings: 1
Location: Falls Church,  VA    USA
Position Description: Clinical Research Management - Financial Management/Research Billing:
• Assists in the coordination of financial aspects of clinical trial implementation from protocol feasibility through to study closure.
• Comply with internal and external reporting of financial aspects including but not limited to research billing in EPIC.
• Coordination with external facilities regarding orders to be billed to research studies instead of insurance or patient.

Quality Assurance/Regulatory Compliance:
• Utilizes and adheres to Inova standards, GCP and FDA guidelines to ensure the highest quality research within Inova.
• Intensive organizational skills and ability to conform to local organizational standards or to suggest and implement improvements.
• Ability and knowledge to identify and suggest solutions to potential quality assurance/regulatory compliance issues as well as prevent them in the future.

• Communicates effectively and works in collaboration with the research team in order to meet research study and departmental objectives. Demonstrates respect and understanding of other clinical disciplines.
• Implement and maintain effective communication and relationships with internal customers including but not limited to 10-15 investigators as well as their office staff members, 4 research team members, and all other surgical staff members.
• Implement and maintain effective communication and relationships with outside representatives from sponsors and granting agencies.

Professional Development/Experience:
• Makes a continuous effort to foster self-development, enhance work related skills and improve job performance and expertise.
• Proficiency in IV starts, venipuncture, and all bio-specimen collection procedures.
• Utilizes critical thinking skills and ongoing nursing assessment for all study participants.
• Implement medication management protocols per study requirements.
• Able to lead evidence based practice educational initiatives for non- clinical learners.
• Knowledge and ability to navigate and work within sterile operating room environment.
• Provides coordination of study subject visit appointments to adhere to protocol specific guidelines.
• Communicates effectively with Principal Investigators/Sub-Investigators.

Qualifications: Other Qualifications:
• Preferred current certification or qualification for certification through ACRP or SOCRA.
• Preferred at least 2 years coordinating medical and/or device studies sponsored by pharmaceutical/device companies and/or government grants.
• Preferred Master’s in scientific field of study, but at least Bachelor’s in a scientific field of study required.

Organization Description:

Closing Date: 12/4/2017
Desired Starting Date:
Contact Name: Sarah Wright,  Clinical Research Nurse
Contact Location:

Contact Location:
Contact Phone: 703-776-3778 
Contact Fax:
Contact Email:
Web Address:
How to Apply:

Additional Information:

Web Site Delete Date: 12/4/2017