h3Clinical Research Coordinator in Milano /h3 h3Working Hours /h3 p20 hours per week /p h3Start Date /h3 pImmediately /p h3Duration /h3 pApproximately 6 months /p pIQVIA is currently recruiting a dedicated Clinical Research Coordinator to support a clinical research site in Rome. This b20h hour per week /b role offers a unique opportunity to contribute to meaningful research in a collaborative and dynamic environment. /p h3Key Responsibilities /h3 pAs a vital member of the site team, you will help ensure the smooth execution of the clinical trial by performing a range of administrative and clinical support tasks, including: /p ul liPrescreening and Screening tasks /li liReview charts from the site data base /li liMaintaining and updating study documentation, including protocols, case report forms (CRFs), Electronic Data Capture (EDC) systems and eTMFs /li liSupporting patient screening and enrollment, including handling informed consent and privacy documentation /li liIP - site accountability including IP - patient compliance /li liUse of IRT/IWRS systems for subject randomization, investigational product assignment, inventory management, and site-level clinical trial operations /li liProcessing and shipment of lab samples process /li liPatient scheduling support /li liPrinting and certifying EMR /li liCoordinating logistical activities for study procedures in line with the study protocol /li liCommunicating with study monitors and responding to study-related inquiries /li liCarrying out general administrative tasks related to the study /li /ul h3Your Profile /h3 pWe are looking for candidates who bring a combination of education, experience, and skills: /p ul liBachelor’s degree in life sciences or equivalent education and/or relevant experience in a clinical or medical setting (e.g., clinical research coordinator, research assistant, nurse, medical assistant) /li liSolid understanding of clinical trials and familiarity with study protocols, consent forms,
and schedules /li liExperience with lap samples and IRT/IWRS systems /li liGood knowledge of medical terminology /li liStrong IT skills, including proficiency in MS Office applications (Outlook, Word, Excel, Access) /li libMust have at least 2 years experience working as a Clinical Research Assistant, Research Nurse or Clinical Research Coordinator at a clinical trial site /b /li liExcellent interpersonal and communication skills /li liStrong organizational skills and attention to detail /li liFluency in English /li /ul h3Why Join IQVIA? /h3 pAt IQVIA, you will be part of a global team that is advancing healthcare through data, technology, and human science. We offer a supportive work environment, impactful projects, and the opportunity to make a real difference. /p p#LI-HCPN /p p#LI-CES /p p#LI-DNP /p p#LI-NS /p p#LI-Onsite /p pIQVIA is a leading global provider of clinical research services, commercial insights and healthcare intelligence to the life sciences and healthcare industries. We create intelligent connections to accelerate the development and commercialization of innovative medical treatments to help improve patient outcomes and population health worldwide. Learn more at /p pIQVIA is committed to integrity in our hiring process and maintains a zero tolerance policy for candidate fraud. All information and credentials submitted in your application must be truthful and complete. Any false statements, misrepresentations, or material omissions during the recruitment process will result in immediate disqualification of your application, or termination of employment if discovered later, in accordance with applicable law. We appreciate your honesty and professionalism. /p pThe potential base pay range for this role, when annualized, is €29,800.00 - €44,800.00. The actual base pay offered may vary based on a number of factors including job‑related qualifications such as knowledge, skills, education, and experience; location; and/or schedule (full or part‑time). Dependent on the position offered, incentive plans, bonuses, and/or other forms of compensation may be offered, in addition to a range of health and welfare and/or other benefits. /p #J-18808-Ljbffr
📌 Clinical Research Coordinator - part time (Rodano)
🏢 Iqvia
📍 Rodano