Job Description

Baptist Health is the region's largest not-for-profit healthcare organization, with 12 hospitals, over 28,000 employees, 4,500 physicians and 200 outpatient centers, urgent care facilities and physician practices across Miami-Dade, Monroe, Broward and Palm Beach counties. With internationally renowned centers of excellence in cancer, cardiovascular care, orthopedics and sports medicine, and neurosciences, Baptist Health is supported by philanthropy and driven by its faith-based mission of medical excellence. For 25 years, we've been named one of Fortune's 100 Best Companies to Work For, and in the [click to reveal phone number]2024-2025 U.S. News & World Report Best Hospital Rankings, Baptist Health was the most awarded healthcare system in South Florida, earning 45 high-performing honors.

What truly sets us apart is our people. At Baptist Health, we create personal connections with our colleagues that go beyond the workplace, and we form meaningful relationships with patients and their families that extend beyond delivering care. Many of us have walked in our patients' shoes ourselves and that shared experience fuels out commitment to compassion and quality. Our culture is rooted in purpose, and every team member plays a part in making a positive impact - because when it comes to caring for people, we're all in.

Description

Supports the professional role of the Clinical Research staff at the Cardiac and Vascular Institute (MCVI) by coordinating and administering the clinical study protocols (CSP) 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:
Supports the professional role of the Clinical Research staff at the Cardiac and Vascular Institute (MCVI) by coordinating and administering the clinical study protocols (CSP) 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.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 of RN ResearchDegrees:

• 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 of RN Research

Job Tags

Full time,

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