Clin Research Nurse II AES

Clinical Research Coordinator / Nurse Coordinator Adecco Healthcare & Life Sciences is hiring for a notable global clinical research organization supporting Phase I-IV clinical studies and advancing innovative therapies through patient-centered research. Location: Katy, TX (Onsite) Pay Rate: $Up to 40.24/hour Duration: 6-Month Contract Potential for Extension: Assignment may be extended based on performance and business needs. Position Summary We are seeking an experienced Clinical Research Coordinator / Nurse Coordinator to support ongoing clinical trials involving both patients and healthy volunteers. This role is responsible for ensuring the successful execution of clinical studies while maintaining participant safety, protocol compliance, data integrity, and regulatory adherence. The ideal candidate will have prior experience independently conducting subject visits, utilizing EDC and IRT systems, and managing study activities from participant recruitment through study completion. Key Responsibilities Conduct clinical research studies in accordance with FDA regulations, ICH-GCP guidelines, study protocols, and site SOPs. Independently perform participant visits, including screening, informed consent, enrollment, and follow-up activities. Execute protocol-specific procedures, including: Vital signs ECGs Height and weight measurements Pregnancy testing Additional clinical assessments as required by protocol Ensure participant safety, comfort, understanding, and compliance throughout the study. Schedule and manage subject visits within protocol-defined timelines and windows. Accurately document clinical data and maintain complete source documentation. Enter and manage study data in Electronic Data Capture (EDC) systems and sponsor platforms within required timelines. Support Interactive Response Technology (IRT) system activities as required. Maintain participant files and ensure all records remain accurate, complete, and audit-ready. Assist with investigational product accountability and related documentation when applicable. Collaborate with investigators, sponsors, monitors, and cross-functional site teams to ensure study success. Support participant recruitment, retention, and follow-up initiatives. Attend site initiation visits, protocol training sessions, investigator meetings, and sponsor-related meetings. Ensure Institutional Review Board (IRB) requirements are met throughout study conduct. Identify, document, and report protocol deviations or suspected non-compliance according to established procedures. Maintain a clean, organized, and compliant clinical research environment. Required Qualifications Bachelor's degree or equivalent combination of education and relevant clinical experience. Active and unrestricted nursing license (RN, LVN, or LPN). Minimum of 1-2 years of experience as a Clinical Research Coordinator, Nurse Coordinator, or related clinical research professional. Experience independently conducting participant visits within clinical trials. Hands-on experience with Electronic Data Capture (EDC) systems. Experience utilizing Interactive Response Technology (IRT) systems.