Local Contractor Research Nurse (Per Diem) Milan Italy Illingworth Research Group provides patient focused clinical services to the pharmaceutical, healthcare, biotechnology and medical device industries, including mobile research nursing, patient concierge, medical photography and clinical research services. Illingworth Research Group is a global organization operating in over 45 countries, bringing clinical research directly into the home of the patient to improve their experience and quality of life. Job Responsibilities Roles within the Research Nurse/Patient Concierge job family are responsible for supporting patients participating in clinical research studies by coordinating care and facilitating communication with healthcare providers. Help patients understand study protocols, schedule appointments, and address concerns. Collaborate with research teams to monitor patient progress and collect data while ensuring compliance with regulatory standards. Serve as a resource to help patients navigate the healthcare system and access necessary services. Manage processes and programs, may oversee a small team, and contribute to the design, implementation, or delivery of processes, programs, and policies. Experience with ports and central venous catheter. Fully conversant with trial protocol, CRFs/eCRFs, off‑site manual, supporting documents, procedures and timelines. Communicate effectively with the Illingworth research nurse project manager, research nurse manager, site staff and the Principal Investigator. Maintain accurate documentation and electronic data transfer per SOPs, ensuring confidentiality and GCP compliance. Attend Site Initiation Visits and other necessary meetings. Coordinate and complete subject trial visits on‑ and off‑site, ensuring procedures and assessments are completed per protocol and SOPs. Administer trial medication per protocol, and facilitate safe storage, transfer and accountability. Process, package and dispatch samples in line with project requirements. Assist in identifying eligible patients and recruiting into trials, providing information and support. Ensure accurate reporting of adverse events (AEs) and serious adverse events (SAEs)/suspected unexpected serious adverse reactions (SUSARs). Report any suspected misconduct or fraud to Illingworth and associated companies. Qualifications Registered nurse with a minimum of 2 years post‑qualification experience. Research and clinical trials experience with GCP certification. Knowledge of research design and methodology desirable. Experience with Venepuncture and ECG. Ability to work autonomously and initiate within a multidisciplinary team. Excellent verbal and written communication skills. Ability to prioritize and manage multiple tasks. Proficiency with Outlook, Word, Excel, and PowerPoint. Additional Information Tasks, duties, and responsibilities are not exhaustive. The Company may assign other tasks at its discretion. Equivalent experience, skills, and education will be considered. Employer is committed to compliance with the Americans with Disabilities Act and EU Equality Directive. #J-18808-Ljbffr