Clinical Research Coordinator
hace 1 día
Torpoint
Join IQVIA as a Clinical Research Coordinator! Are you passionate about clinical research and ready to make a real impact? Do you want to be part of a global leader in healthcare innovation? If so, we’d love to hear from you! IQVIA is seeking a dedicated Clinical Research Coordinator to join our team in Torpoint, working 24 hours per week on a one year contract. This is a fantastic opportunity to contribute to cutting-edge clinical trials at a single site, supporting investigators and ensuring smooth study operations. What You’ll Be Doing: As a key member of the site team, you’ll play a vital role in supporting clinical research activities. Your responsibilities will include: • Supporting clinical studies in line with health and safety policies under the guidance of the Principal Investigator., • Maintaining study documentation including protocols, CRFs, and EDC systems., • Coordinating logistics for study schedules., • Assisting with data entry, quality checks, and resolving queries to ensure accuracy., • Supporting patient recruitment and eligibility screening. What We’re Looking For: We’re seeking someone who is proactive, detail-oriented, and passionate about clinical research. Ideally, you’ll bring: • At least 2 years’ experience as a Clinical Research Coordinator, Research Nurse, or Site Research Assistant., • Solid understanding of clinical trials and study-specific procedures., • Basic knowledge of medical terminology., • Strong IT skills, including MS Office (Access, Outlook, Excel, Word)., • Excellent interpersonal and communication skills., • Strong organisational abilities and attention to detail. Why IQVIA? At IQVIA, you’ll be part of a collaborative and forward-thinking team that’s shaping the future of healthcare. We offer a supportive environment, meaningful work, and the chance to grow your career in clinical research.