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 The Clinical Trials Nurse effectively conducts assigned operations of research protocols. Coordinates, evaluates and follows patient participation in clinical trials. Performs protocol specific clinical tasks including patient assessment, screening, ordering tests, collecting specimens and monitoring responses to the investigational treatment. Implement the standards for research protocols in compliance with regulatory, institutional and external agencies. Work within a Nurse-APRN-Physician ambulatory care model. Performs patient and family education / support. Collaborates with physicians in determining eligibility of patients for clinical trials. Acts as an expert consultant to investigators and others to ensure that Good Clinical Practice (GCP) standards and Standard Operating Procedures (SOP's) are followed. Provides education to staff and patients on disease pathophysiology, treatment plans and clinical trial information. Identify patient problems and recommend plan of care.
The estimated pay range for this position is $40.40 - $53.73 / hour depending on experience.
Qualifications: The Clinical Trials Nurse effectively conducts assigned operations of research protocols. Coordinates, evaluates and follows patient participation in clinical trials. Performs protocol specific clinical tasks including patient assessment, screening, ordering tests, collecting specimens and monitoring responses to the investigational treatment. Implement the standards for research protocols in compliance with regulatory, institutional and external agencies. Work within a Nurse-APRN-Physician ambulatory care model. Performs patient and family education / support. Collaborates with physicians in determining eligibility of patients for clinical trials. Acts as an expert consultant to investigators and others to ensure that Good Clinical Practice (GCP) standards and Standard Operating Procedures (SOP's) are followed. Provides education to staff and patients on disease pathophysiology, treatment plans and clinical trial information. Identify patient problems and recommend plan of care.
The estimated pay range for this position is $40.40 - $53.73 / hour depending on experience.Degrees:
- Bachelors Degree in Nursing is required.
Licenses & Certifications:
- Basic Life Support.
- ACRP Certified Clinical Research Associate.
- SOCRA Certified Clinical Research Professional.
- Collab Inst Training Init.
- ONS/ONCC Chemotherapy Immunotherapy Certificate.
- Registered Nurse.
Additional Qualifications:
- BSN-Bachelors degree in Nursing.
- RNs hired after 2/2012 with an Associate degree will have 5 years from their date of hire to complete the BSN degree.
- CITI must be obtained within the first 30 days of employment.
- ONS chemotherapy certificate must be obtained within first 6 months of employment, Association of Clinical Research Professional (ACRP) Certification or Certified Clinical Research Professional (CCRP) Certification within 1 year of employment.
- 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.
- 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.
- Effective communicator, approachable and comfortable with diverse groups of people.
- Aware and abide by all standards that govern good clinical practices and general nursing practice.
Minimum Required Experience: 2 years of research experience.Degrees:
- Bachelors Degree in Nursing is required.
Licenses & Certifications:
- Basic Life Support.
- ACRP Certified Clinical Research Associate.
- SOCRA Certified Clinical Research Professional.
- Collab Inst Training Init.
- ONS/ONCC Chemotherapy Immunotherapy Certificate.
- Registered Nurse.
Additional Qualifications:
- BSN-Bachelors degree in Nursing.
- RNs hired after 2/2012 with an Associate degree will have 5 years from their date of hire to complete the BSN degree.
- CITI must be obtained within the first 30 days of employment.
- ONS chemotherapy certificate must be obtained within first 6 months of employment, Association of Clinical Research Professional (ACRP) Certification or Certified Clinical Research Professional (CCRP) Certification within 1 year of employment.
- 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.
- 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.
- Effective communicator, approachable and comfortable with diverse groups of people.
- Aware and abide by all standards that govern good clinical practices and general nursing practice.
Minimum Required Experience: 2 years of research experience.
Job Tags
Full time,