Clinical Research Coordinator - part time

In breve

IQVIA is seeking a part‑time Clinical Research Coordinator to support a clinical trial site in Verona. IQVIA is a global provider of clinical research services, commercial insights and healthcare intelligence, helping to accelerate the development of innovative medical treatments worldwide. The role is 24 hours per week, starts immediately and is expected to run for about nine months. In this position you will be a key member of the site team, handling a mix of administrative and clinical support duties. Daily tasks include prescreening and screening participants, reviewing site database charts, and maintaining study documentation such as protocols, case report forms, electronic data capture (EDC) records and electronic trial master files (eTMFs). You will also assist with patient enrollment, manage informed‑consent and privacy paperwork, operate IRT/IWRS systems for randomisation and investigational product handling, schedule patient visits, coordinate logistics for study procedures, and act as a point of contact for study monitors and other inquiries. General administrative responsibilities related to the trial are also part of the role. The ideal candidate holds a bachelor's degree in life sciences or an equivalent qualification and has at least two years of experience working as a Clinical Research Assistant, Research Nurse or Clinical Research Coordinator at a trial site. A solid grasp of clinical‑trial processes, study protocols, consent forms and scheduling is required, as is familiarity with lap samples and IRT/IWRS systems. Strong medical‑terminology knowledge, excellent interpersonal and communication skills, and a high level of organisation and attention to detail are essential. Proficiency with Microsoft Office applications (Outlook, Word, Excel, Access) and fluency in English are also mandatory. Joining IQVIA offers the chance to work within a collaborative, data‑driven environment that values integrity and impact. The role provides a supportive setting, exposure to meaningful research projects and the opportunity to contribute to advances in patient outcomes. Compensation is outlined as an annualised base‑pay range of €29,800, €44,800, with potential additional incentives and a suite of health and welfare benefits. What the role asks for: - Bachelor's degree in life sciences or equivalent - Minimum 2 years experience as Clinical Research Assistant, Research Nurse or Coordinator - Fluency in English - Experience with lap samples - Experience with IRT/IWRS systems - Strong knowledge of medical terminology - Proficiency in MS Office (Outlook, Word, Excel, Access) - Solid understanding of clinical trial processes and documentation