Full-Time

Clinical Research Nurse 2

Updated on 8/1/2026

University of Miami

University of Miami

No salary listed

Company Does Not Provide H1B Sponsorship

Miami, FL, USA

In Person

Category
Medical, Clinical & Veterinary (1)
Biology & Biotech (1)
Required Skills
Phlebotomy
Medication Administration
Nursing
Patient Care
Electronic Health Records (EHR)
Vital Signs
HIPAA
Basic Life Support (BLS)

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Requirements
  • A Bachelor of Science in Nursing from an accredited nursing program is required.
  • A current Florida Registered Nurse license is required.
  • Current American Heart Association Basic Life Support certification for healthcare providers is required.
  • An Oncology Nursing Society provider card for chemotherapy and immunotherapy administration certification is required.
  • A minimum of 3 years of relevant experience is required.
  • Candidates must demonstrate strong communication, collaboration, time management, critical-thinking, analytical, problem-solving, reading, writing, mathematical, organizational, and comprehension skills.
  • Candidates must be knowledgeable about patient care, including assessing, planning, coordinating, monitoring, and evaluating patient progress through the continuum of care.
  • Candidates must be knowledgeable in navigating electronic medical records and reviewing treatment plans.
  • Candidates must uphold professional ethics, maintain patient confidentiality, and accurately complete assignments.
  • Candidates must be able to work evenings, nights, and weekends as necessary.
  • Candidates must be able to work independently and collaboratively in a clinical research environment.
Responsibilities
  • Deliver patient-family centered care in an ambulatory setting while complying with clinical research protocols, practice guidelines, federal and sponsor regulations, and institutional policies.
  • Recruit research participants and support achievement of research objectives.
  • Perform the nursing process, including assessing and screening patients, interpreting data, planning and implementing care, evaluating outcomes, coordinating care, and teaching patients and families.
  • Monitor nursing quality and promote a compassionate, culturally competent care environment.
  • Delegate tasks appropriately, follow up on completion, provide constructive feedback, and serve as a clinical role model, mentor, and preceptor.
  • Assess patients, determine nursing diagnoses, modify treatment plans, and implement and evaluate nursing and medical interventions.
  • Perform patient tests, administer medications, maintain treatment records, and monitor for adverse responses and side effects.
  • Use telephone, mobile smart device, web-based, and digital technology platforms for communication, documentation, and telehealth services when applicable.
  • Assess learning needs and teach patients, families, staff, and subjects about self-care, illness prevention, protocols, treatments, side effects, and complications.
  • Activate emergency protocols and respond appropriately to rapidly changing situations.
  • Monitor patient and employee safety, compliance with standards and policies, and opportunities for continual improvement.
  • Prioritize and coordinate multiple requests, participate in unit programs and meetings, and contribute to team building and conflict resolution.
  • Communicate plans of care and research information to patients, families, investigators, clinical staff, and other care-team members while complying with HIPAA and transition-of-care requirements.
  • Participate in shared governance, professional development, publications, presentations, and other professional activities.
  • Provide clinical trial support in hospital and clinic settings according to Good Clinical Practice standards.
  • Screen patients and records for potential trial candidates and notify treating physicians and clinical research staff.
  • Assist investigators with subject informed consent and answer clinical-trial questions within the nursing scope of knowledge.
  • Assess and document adverse events, concomitant medications, patient compliance, and response to protocol treatment.
  • Ensure serious adverse events are documented and reported according to protocol and regulatory requirements.
  • Prepare and review data for monitoring visits, audits, and safety summaries, and support clinical audits through preparation, participation, documentation, and follow-up.
  • Provide informed consent documents and source documentation needed to determine eligibility and maintain compliance.
  • Review clinical trial treatment order sets and individual patient orders with investigators, investigational pharmacists, treatment-unit staff, and clinical research leadership.
  • Enter research-related orders, tests, and procedures into patient charts for investigator signature.
  • Perform protocol-specific electrocardiograms, research blood draws, vital signs, and other simple clinical tasks within scope and competency.
  • Coordinate communication among physicians, allied health professionals, nursing staff, clinical trial patients, families, and research staff regarding trial-related issues.
  • Ensure protocol-related education is effective for patients and multidisciplinary team members.
  • Ensure clinical trial procedures are performed according to protocol and administer investigational oral medication received from pharmacy, with appropriate documentation.
  • Perform a second chemotherapy order check before administration by another clinical trials nurse.
  • Attend investigator meetings, maintain a safe working environment, and report safety variances.
  • Implement Corrective Action and Preventive Action assessments and follow related issues through resolution.
  • Mentor and encourage clinical research staff through professional organizations, committees, journal presentations, seminars, and conferences.
Desired Qualifications
  • Certification in a relevant specialty or field, such as oncology or clinical research, is preferred.

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