Senior Clinical Research Nurse

Job Description:The Clinical Research Nurse I is responsible for conducting clinical study procedures in compliance with study protocols, Good Clinical Practice guidelines, and regulatory standards.This role ensures participant safety, accurate documentation, and effective coordination with the Principal Investigator and clinical study team to support successful study execution. Essential Functions:Perform study procedures in strict compliance with study protocols, Good Clinical Practice standards, SOPs, QA/QC procedures, OSHA guidelines, and applicable regulations.Monitor and ensure the safety and well-being of study participants through active assessment and continuous presence.Facilitate verbal directions from the Principal Investigator to study participants and clinical staff and ensure appropriate follow-through.Assist the Principal Investigator in reviewing laboratory data for participant selection, randomization, and safety monitoring.Assess participants to identify Adverse Events, ensure proper documentation and reporting, and provide appropriate clinical care as directed or deemed necessary.Communicate study progress regularly to the Principal Investigator, Clinical Study Manager, and study team.Immediately notify leadership of any Serious Adverse Events and initiate required documentation.Enforce study rules and handle participant concerns professionally while maintaining satisfaction.Maintain compliant, clear, and accurate study charts including Adverse Events and Concomitant Medication documentation.Serve as floor leader and mentor in the absence of the Clinical Study Manager, supporting research and laboratory staff.Demonstrate leadership and professionalism within the clinical study team.Administer study medications and concomitant medications per protocol and maintain accurate documentation.Coordinate with scheduling to ensure proper coverage of clinical conduct activities.Provide protocol training and real-time performance feedback in collaboration with management.Oversee End of Study and Early Termination procedures including follow-up on outstanding items after discharge.Provide administrative and operational support to ensure successful protocol execution. Qualifications Education:Nursing degree with active in-state licensure required. Experience:One to two years of experience in a clinical research environment required.Equivalent combination of education and experience may be considered. Certification and Licensure:Advanced Life Support certification required. Knowledge, Skills, and Abilities:Strong leadership skills.Excellent customer service and public relations experience.Professional verbal and written communication skills with diverse populations.Ability to work independently and manage competing priorities.Strong multitasking skills in deadline-driven environments.Ability to function effectively within a team setting.Excellent organizational skills, time management, and attention to detail. Physical Requirements and Working Conditions:Ability to sit, stand, walk, stoop, bend, and lift materials up to 50 pounds for extended periods as required.