Clinical Research Coordinator Registered Nurse

• Benefits from Day One:
  Medical, Dental, Vision Insurance, Life Insurance, Disability Insurance
• Paid Time Off from Day One
• 403-B Retirement Plan
• 4 Weeks 100% Paid Parental Leave
• Career Development Whole Person Well-being Resources Mental Health Resources and Support Pet Benefits

Full time Shift: Day (United States of America)

200 N LAKEMONT AVE City: WINTER PARK State:
Florida Postal Code: 32792

• Executes and coordinates the informed consent process for participants in clinical trials and research studies.
• Screens potential research participants to determine eligibility for clinical trials and studies.
• Provides detailed information about the study, including its purpose, procedures, risks, and benefits, to potential participants.
• Ensures that participants fully understand the informed consent document before they sign it, and clarifies any questions or concerns.
• Maintains accurate and complete records of the informed consent process, including signed consent forms and documentation of discussions.
• Coordinates or performs biospecimen collection and maintains HIPAA protected database connecting patient information to biospecimens used in research.
• Serves as the study‑specific clinical point of contact for participants, investigators, research staff, hospital departments and external research partners.
• Maintains sensitivity to cost containment measures by conserving hospital supplies and human resources while overseeing proposed project budgets.
• Conducts research regarding patient screening and clinical eligibility assessments.
• Coordinates the care and follow‑up of volunteers placed on research studies, trials, and programs.
• Provides ongoing support and information to participants throughout the duration of studies.
• Works flexible hours and is available for research project‑related questions.
• Ability to perform clinical tasks including assisting physician, ARNP and CRN with minor procedures and other study requirements within scope of practice.
• Ability to work independently in a fast‑paced clinical or research environment, handling multiple tasks simultaneously, effectively, and in an organized and timely manner.
• Demonstrated skills in clinical competencies including physical assessment, phlebotomy, IV insertion and administration of investigational drugs in accordance with Advent Health Policies and Procedures.
• Other duties as assigned.

• Ability to perform clinical tasks including assisting physician, ARNP and CRN with minor procedures and other study requirements within scope of practice.
• Ability to work independently in a fast‑paced clinical or research environment, handling multiple tasks simultaneously, effectively, and in an organized and timely manner.
• Ability to acclimate and integrate into various clinical settings as needed per protocol.
• Demonstrated skills in clinical competencies including physical assessment, phlebotomy, IV insertion and administration of investigational drugs in accordance with Advent Health Policies and Procedures.
• Knowledge of HIPAA data protection and patient advocacy or similar awareness of ethical treatment of participants in research.
• Ability to communicate effectively with research participants, investigators, research staff and external partners.
• Ability to apply analytical approach to problem solving, obtain and analyze facts, and apply sound judgement.
• Ability to accept direction and respond to the changing needs of clinical research units.
• Working knowledge of Microsoft Office applications, such as, Word, Excel, Access, Outlook, and Internet knowledge and skill.
• Specialized knowledge of the unique needs of patients in the assigned therapeutic areas undergoing treatment (Preferred).
• Specialized knowledge of…