Clinical Research RN - 252716

Benefits

Qualifications

• •Bachelor of Science in Nursing (BSN)
• •Experience in critical care, acute care, or clinical research
• •Active BLS and ACLS certifications
• •Ability to work 12-hour overnight shifts
• •1 more items(s)

Responsibilities

• •Administer study medications as prescribed and perform clinical procedures including phlebotomy, blood draws, and vital sign monitoring in accordance with study protocols
• •Initiate peripheral IV lines without the use of tourniquets, following protocol-specific guidelines
• •Conduct thorough reviews of participants’ current medications and accurately document findings in source documentation
• •Administer concomitant medications as required
• •Support daily clinical operations to ensure efficient workflow and high-quality care for research participants
• •Complete and maintain study source documentation, including cMAR, fluid balance logs, adverse events (AE), and concomitant medication records
• •Monitor and document participant responses to treatment, including identifying and reporting adverse events (AE/SAE), and completing required intake forms
• •Identify and resolve discrepancies within study documentation
• •Maintain adequate inventory of clinical supplies and consumables
• •Assist with onboarding and training of new staff, including skills assessment and protocol education
• •Provide oversight and guidance to Research Assistants and technical staff on nursing-related study procedures, including specimen collection and handling
• •Support compliance-related processes in partnership with Human Resources, including exposure incident documentation and follow-up
• •Maintain employee health records, including immunizations (e.g., TB, Hepatitis B)
• •Develop study-specific reference materials and summaries for nursing and research staff
• •Participate in ongoing training and education for clinical staff related to study protocols and procedures
• •Overnight shifts: 6:00 PM – 6:00 AM
• •13 more items(s)