Clinical Research Coordinator - part time

In breve

IQVIA is seeking a part‑time Clinical Research Coordinator to support a trial site in Rome. IQVIA is a global provider of clinical research services, data analytics and healthcare intelligence that helps bring new medical treatments to market. The role is a 20‑hour‑per‑week contract lasting roughly six months, with an immediate start. The coordinator will handle a blend of administrative and clinical duties to keep the study running smoothly. Core tasks include prescreening and screening participants, reviewing site database charts, and maintaining study documents such as protocols, case report forms, electronic data capture entries and electronic trial master files. The role also involves assisting with patient enrollment, managing informed‑consent paperwork, overseeing investigational‑product accountability and compliance, and using IRT/IWRS systems for randomisation and inventory control. Additional responsibilities cover processing and shipping laboratory samples, scheduling patients, printing and certifying electronic medical records, coordinating logistics for study procedures, and responding to monitor queries and other study‑related communications. Candidates must hold a bachelor's degree in life sciences or an equivalent qualification, or possess comparable experience in a clinical environment. At least two years of experience as a Clinical Research Assistant, Research Nurse or Clinical Research Coordinator at a trial site is required. Applicants need solid familiarity with clinical‑trial protocols, consent forms and schedules, as well as hands‑on experience with lab samples and IRT/IWRS platforms. Proficiency in medical terminology and strong IT skills, including Microsoft Outlook, Word, Excel and Access, are essential. Excellent interpersonal and communication abilities, meticulous organisational skills and fluency in English are also mandatory. IQVIA offers the chance to join a worldwide team that leverages data, technology and human science to improve patient outcomes. The position provides a supportive environment, exposure to impactful research projects and the possibility to make a tangible contribution to healthcare advancement. The role is based in Rome, with a part‑time schedule of 20 hours per week and a competitive salary range of €29,800‑€44,800 annually, adjusted for experience and location. Additional incentive plans, bonuses and health‑welfare benefits may be available depending on the final offer. What the role asks for: - Bachelor's degree in life sciences or equivalent - Minimum 2 years experience as Clinical Research Assistant/Coordinator - Experience with lab sample handling - Experience with IRT/IWRS systems - Strong knowledge of medical terminology - Proficiency in MS Office (Outlook, Word, Excel, Access) - Excellent interpersonal and communication skills - Fluency in English - Strong organisational skills and attention to detail