Clinical Research Nurse

Job Title: Clinical Research Nurse I (Day Shift) Location: Overland Park, KS – Contract Position The Clinical Research Nurse I plays a key role in ensuring the safety, comfort, and informed consent of clinical trial participants while supporting the successful execution of study protocols. Responsibilities include performing clinical trial procedures, maintaining safety equipment readiness, and mentoring the Clinical Operations team. The position is based in a clinical research unit in the suburb of Overland Park, KS and follows a Monday–Friday day shift schedule. Responsibilities Ensure the safety and informed consent of clinical trial participants throughout the course of each study. Carry out clinical trial procedures in accordance with study protocols, Good Clinical Practice (GCP) guidelines, and Standard Operating Procedures (SOPs). Perform ongoing monitoring and safety evaluations for clinical trial participants. Administer investigational products (IP) as directed by study protocols. Perform catheter placement and other required clinical procedures within the scope of practice. Safeguard the privacy and confidentiality of all clinical trial participants and sponsor information at all times. Serve as a mentor and resource to members of the Clinical Operations team, offering guidance and support as needed. Identify opportunities to improve safety practices and communicate recommendations to department leadership. Observe, document, and ensure appropriate follow‑up for any participant adverse events, in alignment with study and safety requirements. Coordinate Basic Life Support (BLS) and Advanced Life Support (ALS) training sessions for Clinical Operations staff, as needed. Promote and uphold high standards of customer service, quality, and patient safety within the department. Support study‑related informed consent processes during participant screenings when required. Provide training to staff on clinical trial processes relevant to their roles and responsibilities. Communicate study updates and progress to appropriate team members to support effective collaboration. Proactively escalate issues related to participant safety, protocol adherence, or operational challenges and share potential solutions with supervisors and management. Assist with pre‑screening patients for eligibility based on study criteria. Support patient recruitment activities for clinical trials. Conduct chart reviews to identify potential participants and to verify study‑related information. Essential Skills Active Registered Nurse (RN) license with eligibility to practice in Kansas. Ability to perform clinical procedures such as monitoring, safety evaluations, investigational product administration, and catheter placement within the RN scope of practice. Strong commitment to maintaining participant privacy and confidentiality. Ability to follow detailed study protocols, GCP guidelines, and SOPs with high attention to detail. Capability to observe, document, and follow up on adverse events accurately and promptly. Effective communication skills for interacting with participants, colleagues, and interdisciplinary teams. Ability to mentor and serve as a resource to Clinical Operations staff. Organizational skills to manage multiple study‑related tasks and responsibilities. Basic Life Support (BLS) certification or ability to obtain and maintain BLS certification. Capacity to coordinate and support BLS and ALS training sessions for staff. Ability to work the specified day shift schedule (0600–1430, Monday–Friday). Additional Skills & Qualifications No prior clinical research experience is required; training will be provided. Advanced Life Support (ALS) certification is not required; support is available to help recertify if needed. Experience with pre‑screening patients and patient recruitment is beneficial. Familiarity with chart review processes is an advantage. Interest in clinical research and willingness to learn study‑specific procedures and documentation requirements. Ability to contribute to a culture of high‑quality patient care, safety, and customer service. Employment Type & Schedule Contract position. Standard schedule is Monday through Friday, 6:00 am–2:30 pm. Pay $39.00–$40.00 per hour. Benefits Medical, dental & vision Critical Illness, Accident, and Hospital 401(k) Retirement Plan – Pre‑tax and Roth post‑tax contributions available Life Insurance (voluntary life & AD&DD for the employee and dependents) Short‑term and long‑term disability Health Spending Account (HSA) Transportation benefits Employee Assistance Program Time Off/Leave (PTO, vacation, or sick leave) Application Deadline Position anticipated to close on Jul 17, 2026. Equal Opportunity Statement The company is an equal‑opportunity employer and will consider all applications without regard to race, sex, age, color, religion, national origin, veteran status, disability, sexual orientation, gender identity, genetic information or any characteristic protected by law. Reasonable Accommodation If you would like to request a reasonable accommodation, such as modification or adjustment of the job application process or interviewing process due to a disability, please contact the company’s accommodation office at the address provided in the application portal. #J-18808-Ljbffr