Sr. Research Nurse - Cancer Institute (Full Time, Days)

Nicklaushealth; Sunset Corners (FL); On-site; USD 85,000 - 110,000; Full time

Job summary

The Senior Research Nurse at Nicklaus Children's Hospital Research Institute (NCH-RI) operates within a centralized team of specialists to ensure conduct of clinical trials in compliance with applicable regulations and sponsor requirements.

Reporting to the CTO Manager, you will train staff, coordinate study activities, manage data collection and adverse event reporting, and support quality assurance across study teams at Nicklaus Children’s Hospital and affiliated departments.

Qualifications

• Bachelor's Degree in Nursing required and active RN licensure in Florida or compact license.
• APRNs preferred but not required.
• Clinical research experience and regulatory knowledge essential.

Responsibilities

• Coordinates team activities to ensure studies run per protocol and SOPs within budget.
• Plans procedures logistics and risk mitigation for studies.
• Prepares training materials and coordinates staff training and certifications.
• Maintains and monitors protocol compliance, QA, and regulatory reporting.
• Collects, compiles, and analyzes clinical research data across sites.
• Engages with patients and families to facilitate recruitment and consent.
• Assists with study start-up, amendments, and study design input as needed.

Skills

Clinical research

Regulatory compliance

Training & education

Communication skills

Project management

Bilingual English/Spanish

Education

Bachelor's Degree in Nursing

RN Licensure (FL)

Tools

REDCap

EMR systems

MS Office

Job description

Job Summary

The Senior Research Nurse is part of a central team of specialized research professionals within the Nicklaus Children's Hospital Research Institute (NCH-RI). This research position reports directly to the NCH-RI Clinical Trials Office (CTO) Manager but works closely with Lead CRA's, Study Team (PI, Sub-I's, CRC', etc.), NCH-RI departments and Nicklaus Children's 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. Provides direction, support, and guidance to research clients and their families. Develops and implements educational activities pertaining to research, disease prevention, and care to clients, families, staff and the community. Assures excellence in quality, the protection of human subjects, and information management in research activities. Assists Regional Research Manager in research billing and compliance. 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 coordinates 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 Children’s 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 Sponsor’s 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.

Qualifications

Minimum Job Requirements

• Bachelor's Degree in Nursing
• Registered Nurse 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 certification required within 3 months of hire date – maintain active and in good standing throughout employment
• American Heart Association PALS certification required within 6 months of hire date – maintain active and in good standing throughout employment
• 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

• APRN 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 and available to work off-hours depending on the study requirements.