Job Description

Minimum Job Requirements

• BSN Bachelors of Science in Nursing
  
• RN Licensure within the State of Florida or Multi-State Enhanced Nursing License Compact (eNLC) maintain active and in good standing throughout employment
  
• IATA certification completion required within 3 months of hire date
  
• American Heart Association ACLS (Advanced Cardiovascular Life Support) certification required within 2 months of hire
  
• American Heart Association PALS (Pediatric Advanced Life Support) certification completion required within 6 months of hire
  
• American Heart Association BLS - maintain active and in good standing throughout employment
  
• 2-4 years of professional research or healthcare experience
  
• 1-3 years of Phase 1 clinical research experience

Knowledge Skills and Abilities

• ARNP highly preferred
  
• Clinical research certification (e.g. CCRC CCRP CRA) preferred
  
• Bilingual in English/Spanish preferred
  
• Pediatric Nursing experience in an acute care setting preferred
  
• Experience in neurology neurosurgery or oncology preferred
  
• Experienced with database management tools and/or REDCap preferred
  
• In-depth knowledge of Phase I clinical trials
  
• Demonstrated knowledge of clinical research trial design and execution
  
• Experienced with electronic medical record and clinical trial management software applications
  
• Strong written and verbal communication skills
  
• Excellent interpersonal skills
  
• Excellent problem-solving skills
  
• Effective organizational and project management skills
  
• Ability to pay close attention to detail
  
• Ability to comprehend professional and scientific journals
  
• Ability to apply principles of logical and scientific thinking to a wide variety of intellectual and practical problems
  
• Ability to establish and maintain effective working relationships with coworkers managers and clients
  
• Proficiency in Microsoft Office including Access Word Excel Outlook and PowerPoint
  
• Willing to work off-hours depending on the study requirements

Job Summary

The Clinical Research Nurse CTO is part of a central team of specialized research professionals within the Nicklaus Childrens Hospital Research Institute (NCH-RI). This research position reports directly to the NCH-RI Clinical Trials Office (CTO) Manager but works closely with Lead CRAs Study Team (PI Sub-Is CRC etc.) NCH-RI departments and Nicklaus Childrens Hospital (NCH) department administrators and other clinical research professionals to help ensure that clinical research and related activities are performed in accordance with all applicable Federal regulations NCH/NCH-RI applicable policies and sponsor policies/requirements. This research position will also coordinate team activities to ensure studies are carried out according to protocol standard operating procedures (SOPs) and applicable guidelines and regulations.

Job Specific Duties

• Coordinates team activities to ensure studies are carried out according to protocol standard operating procedures (SOPs) applicable guidelines and regulations and within budget.
  
• Plans logistical activity for procedures as per protocol and ensures thorough resource planning. Identifies risks on study and ensures that actions are implemented to mitigate risks identified.
  
• Ensures study specific training materials documents and records are prepared and delivered or coordinate training dry runs simulations and tests as required.
  
• Implements monitors and assesses the need for training programs to maintain staff skill proficiency including annual validation and currency of required certifications and licenses.
  
• Provides protocol-specific training to research study team and NCH hospital/department staff directly involved with the care/treatment of research patients.
  
• Works with NCH-RI staff to assist with developing updating and implementing new Research Standard Operating Procedures guidance documents standard work and work flows (related to early phase research).
  
• Coordinates plans implements and evaluates nursing care to clinical trial study participants including but not limited to Adverse Event reporting and other support activities.
  
• Provides nursing-related care to clinical trial study participants as outlined (and applicable) in the study protocol.
  
• Coordinates and executes the collection compilation and analysis of clinical research data from studies conducted by PIs and study teams at Nicklaus Childrens and the NCH-RI.
  
• Interacts with patients and families to recruit study subjects and ensures compliance with protocol guidelines and requirements of regulatory agencies.
  
• Attends and participates in investigator meetings pre-study visits/initiation or coordinator meetings. Produces quality documentation including completion of assessments within the specified time.
  
• Coordinates and responsible for the collection of blood samples (PK samples and other) cultures tissues and other specimens as required by protocol.
  
• Prepares oral presentations/written reports/data requests describing progress trends and appropriate recommendations or conclusions as it relates to research at Nicklaus.
  
• Communicates with the Sponsor or representatives regarding scheduling and facilitation of study monitor visits and facilitates communication between PI and Sponsor or Sponsors Representatives.
  
• Reviews protocol and provides study feasibility input to the NCH-RI Leadership and Study Start-up Team. Works with QI/QA team to ensure quality standards are being met and reports adverse events protocol deviations.
  
• Ensures compliance of general and study specific regulatory related processes with SOPs FDA NIH and applicable regulations for the reporting of events to regulatory agencies.
  
• Assists with the design and implementation of protocols forms/questionnaires and the preparation of amendments to protocols and/or modifications to study design as appropriate for local Investigator Initiated studies.

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