Cardiovascular Research Nurse, Lynn Heart and Vascular Institute, $15,000 Bonus, FT, 8A-4:30P

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

The Research Nurse is responsible for enlisting, maintaining, and assuring protocol compliance for all patients on clinical trials. Collaborates with physicians in determining eligibility of patients for clinical trials. Provides education to staff and patients. Ensures site research quality by practicing in compliance with standard operating procedures (SOPs), principles of Good Clinical Practice (GCP) and applicable federal, state, and local regulations. Estimated salary range for this position is $[click to reveal phone number]73860.80 - $[click to reveal phone number]96019.04 / year depending on experience.

Qualifications:
The Research Nurse is responsible for enlisting, maintaining, and assuring protocol compliance for all patients on clinical trials. Collaborates with physicians in determining eligibility of patients for clinical trials. Provides education to staff and patients. Ensures site research quality by practicing in compliance with standard operating procedures (SOPs), principles of Good Clinical Practice (GCP) and applicable federal, state, and local regulations. Estimated salary range for this position is $[click to reveal phone number]73860.80 - $[click to reveal phone number]96019.04 / year depending on experience.Degrees:

• Bachelors.

Licenses & Certifications:

• Advanced Cardiovascular Life Support.
• Basic Life Support.
• Collab Inst Training Init.
• Registered Nurse.

Additional Qualifications:

• Clinical Study Coordinator Certification preferred.
• Knowledge of medical terminology, nursing assessment, clinical trials and GCP concepts.
• Experience with computer data entry and database management.
• Excellent written and oral communication skills.
• Must be able to communicate in English and Spanish.
• Excellent organizational skills.
• Attention to details and accuracy.
• Ability to read, analyze, and interpret technical procedures such as protocols, informed consent documents, and regulatory documents.
• Ability to work independently, organize, prioritize, and follow through with results.
• Ability to solve practical problems and implement solutions.
• Must be able to communicate in English and Spanish.

Minimum Required Experience: 3 years experience required. RN, BLS, ACLS, CITI and ONS/ONCC required. CCRC/CCRP certification preferred. CITI required within 30 days. ACRP/CCRP required after 2 years experience.Degrees:

• Bachelors.

Licenses & Certifications:

• Advanced Cardiovascular Life Support.
• Basic Life Support.
• Collab Inst Training Init.
• Registered Nurse.

Additional Qualifications:

• Clinical Study Coordinator Certification preferred.
• Knowledge of medical terminology, nursing assessment, clinical trials and GCP concepts.
• Experience with computer data entry and database management.
• Excellent written and oral communication skills.
• Must be able to communicate in English and Spanish.
• Excellent organizational skills.
• Attention to details and accuracy.
• Ability to read, analyze, and interpret technical procedures such as protocols, informed consent documents, and regulatory documents.
• Ability to work independently, organize, prioritize, and follow through with results.
• Ability to solve practical problems and implement solutions.
• Must be able to communicate in English and Spanish.

Minimum Required Experience: 3 years experience required. RN, BLS, ACLS, CITI and ONS/ONCC required. CCRC/CCRP certification preferred. CITI required within 30 days. ACRP/CCRP required after 2 years experience.