Nurse Research Coordinator, MCVI Research, FT, 8A-4:30P

Clinical Research Coordinator

Supports the professional role of the Clinical Research staff at the Cardiac and Vascular Institute by coordinating and administering the clinical study protocols in cooperation with the Principal Investigator. Perform functions as required by the CSP making sure all requirements are met. Ensures compliance with all regulatory requirements. Must be able to complete detailed paperwork in strict accordance with study specific requirements and all federal and regulatory guidance. Organizing tactical interventions that maximize subject finding, participation, enrollment and retention for cardiovascular research protocols in cooperation with the principal investigators. Performs those functions required by the research director to enroll patients in research protocol within a regulatory framework in accordance with IRB requirements and good clinical practices. Serves as a research advocate to ensure that all enrollment requirements are met while abiding by regulatory requirements and maintaining research protocol demands. Deal with physicians, patients, sponsors and other departments in a service oriented, excellent manner.

Qualifications:

Degrees:

• Associates.

Licenses & Certifications:

• Collab Inst Training Init.
• Registered Nurse.

Additional Qualifications:

• Associates in Science required, BSN in Nursing Highly Preferred but Bachelors on health related field accepted.
• CITI Training is a Must.
• Clinical Study Coordinator Certification Preferred.
• Strong clinical background in critical care/cardiac/cath lab with experience in quality monitoring, and/or research methodology.
• Ability to manage multiple study protocols/projects systematically.
• Excellent interpersonal collaborative and team building skills.
• Must be able to work in highly stressful environments and high volume areas with multi tasking to ensure enrollment of patients in accordance with regulatory requirements.
• Must be able to communicate in Spanish and English, complete detailed paperwork in strict accordance with regulatory requirements and deal with physicians, patients, sponsors and other departments in a service excellence manner.
• Provide in-services to other departments.
• Skills in using word processing and spreadsheet software.
• Knowledge of Research Guidelines and Regulatory Requirements, FDA, NIH, OHRP and the Code of Federal Regulations.

Minimum Required Experience: 2 Years

EOE, including disability/vets