Full-Time

Clinical Research Nurse 2

Posted on 11/22/2025

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)
Requirements
  • Education: Bachelor of Science in nursing required Graduated from an accredited nursing program
  • Experience: Minimum 3 years of relevant experience required
  • Certification and Licensing: Current Florida Registered Nurse license; Current American Heart Association (AHA) Basic Life Support (BLS) for healthcare providers Certification Oncology Nursing Society (ONS) provider card for Chemotherapy and Immunotherapy administration Certification in relevant specialty or field (i.e., oncology, clinical research, etc.) preferred
  • Knowledge, Skills and Abilities: Learning Agility: Ability to learn new procedures, technologies, and protocols, and adapt to changing priorities and work demands.
  • Teamwork: Ability to work collaboratively with others and contribute to a team environment.
  • Technical Proficiency: Skilled in using office software, technology, and relevant computer applications.
  • Communication: Strong and clear written and verbal communication skills for interacting with colleagues and stakeholders.
Responsibilities
  • Assesses, troubleshoots, and reports problems with data collection to appropriate managing staff.
  • Identifies desired research outcomes and evaluates and monitors subjects’ responses.
  • Conducts initiation visits and registers patients in clinical studies.
  • Performs study data collection and entry using charts, correspondence, medical records, and relevant communications. Identifies and procures equipment and supplies needed to fulfill project requirements.
  • Educates staff and subjects about protocols, treatment, possible side effects, and complications. May also collect and handle specimens as required by individual study protocols.
  • Prepares and processes new research proposals and amendments and continually monitors applications and adverse events.
  • Assists with study completion, data lock, study closeout, and archiving of study files to ensure completeness and continuity of all study data.
  • Completes ongoing checks of clinical data entered on the case report forms to ensure accuracy and revises any discrepancies.
  • Adheres to University and unit-level policies and procedures and safeguards University assets.

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