Clinical Research Coordinator

Clinical Research Coordinator Are you seeking an opportunity in Clinical Research? Do you want to work for an industry-leading company? If so, join us – IQVIA is looking for a Clinical Research Coordinator. This part-time role (24 hours) supports a site in Belfast conducting a clinical trial in the respiratory field. As a key member of the site team, you will handle various administrative tasks to support investigators, ensure smooth clinical trial operations, and assist with patient data collection. Day-to-day responsibilities include: Supporting clinical research studies and maintaining a safe environment per health and safety policies under the guidance of the Principal Investigator. Safeguarding participant well-being, acting as a volunteer advocate, and addressing concerns. Keeping study protocols, case report forms (CRFs), Electronic Data Capture (EDC) systems, and other documents current. Planning and coordinating logistics for study procedures per protocol. Preparing for studies, including labeling specimens, inventory management, and troubleshooting equipment. Assisting with data entry, quality checks, and resolving queries to ensure protocol adherence and data accuracy. Supporting study enrollment through recruitment, screening, and participant orientation. Managing study drug custody following standard procedures. Collaborating with study monitors and responding to their questions effectively. Qualifications and skills required: BSc/BA in life sciences or equivalent, or relevant clinical experience (e.g., research coordinator, nurse, medical assistant). Basic understanding of clinical trials, protocols, consent forms, and schedules. Knowledge of medical terminology. Proficiency with MS Windows and Office, including Access, Outlook, Excel, Word. Excellent interpersonal skills for effective teamwork and communication. Strong organizational skills with attention to detail. #J-18808-Ljbffr