Clinical Trials Research Nurse, Clinical Trials, FT, 8A-4:30P Position Available In Miami-Dade, Florida

Tallo's Job Summary: The Clinical Trials Research Nurse at Baptist Health conducts research protocols, coordinates patient participation, and performs clinical tasks. The role involves patient education, collaboration with physicians, and ensuring compliance with standards. The estimated pay range is $40.40 - $53.73 per hour, depending on experience. Qualifications include a Bachelor's degree in Nursing, RN licensure, and certifications in Basic Life Support and Clinical Research.

Company:
Baptist Health
Salary:
$97895
JobFull-timeOnsite

Job Description

Job Description:

Baptist Health is the region’s largest not-for-profit healthcareorganization, with 12 hospitals, over 28,000 employees, 4,500physicians and 200 outpatient centers, urgent care facilities andphysician practices across Miami-Dade, Monroe, Broward and PalmBeach counties. With internationally renowned centers of excellencein cancer, cardiovascular care, orthopedics and sports medicine,and neurosciences, Baptist Health is supported by philanthropy anddriven by its faith-based mission of medical excellence. For 25years, we’ve been named one of Fortune’s 100 Best Companies to WorkFor, and in the 2024-2025 U.S. News & World Report Best HospitalRankings, Baptist Health was the most awarded healthcare system inSouth Florida, earning 45 high-performing honors.

What truly sets usapart is our people. At Baptist Health, we create personalconnections with our colleagues that go beyond the workplace, andwe form meaningful relationships with patients and their familiesthat extend beyond delivering care. Many of us have walked in ourpatients’ shoes ourselves and that shared experience fuels outcommitment to compassion and quality. Our culture is rooted inpurpose, and every team member plays a part in making a positiveimpact – because when it comes to caring for people, we’re allin.

DescriptionThe Clinical Trials Nurse effectively conductsassigned operations of research protocols. Coordinates, evaluatesand follows patient participation in clinical trials. Performsprotocol specific clinical tasks including patient assessment,screening, ordering tests, collecting specimens and monitoringresponses to the investigational treatment. Implement the standardsfor research protocols in compliance with regulatory, institutionaland external agencies. Work within a Nurse-APRN-Physicianambulatory care model. Performs patient and family education /support. Collaborates with physicians in determining eligibility ofpatients for clinical trials. Acts as an expert consultant toinvestigators and others to ensure that Good Clinical Practice(GCP) standards and Standard Operating Procedures (SOP’s) arefollowed. Provides education to staff and patients on diseasepathophysiology, treatment plans and clinical trial information.

Identify patient problems and recommend plan of care. Estimated payrange for this position is $40.40 – $53.73 / hour depending onexperience.

QualificationsDegrees:

Bachelors.

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 5years from their date of hire to complete the BSN degree. CITI must be obtained within the first 30 days ofemployment. ONS chemotherapy certificate must be obtained within first 6months 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, clinicaltrials and GCP concepts. Experience with computer data entry and databasemanagement. Excellent written and oral communication skills. Excellent organizational skills. Attention to details and accuracy. Ability to read, analyze, and interpret technical proceduressuch as protocols, informed consent documents, and regulatorydocuments. Ability to work independently, organize, prioritize, and followthrough with results. Ability to solve practical problems and implementsolutions. Effective communicator, approachable and comfortable withdiverse groups of people. Aware and abide by all standards that govern good clinicalpractices and general nursing practice.

EOE, includingdisability/vets

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