Senior Cra

Job Description Why Join Clinical Functional Service Partnerships (CFSP)? \ N At IQVIA, our Clinical Functional Service Partnership (CFSP) model gives you the best of both worlds: the variety and sponsor-level exposure of working as an embedded member of a leading pharmaceutical or biotechnology team, backed by the stability, global infrastructure, and career support of IQVIA. You'll develop deep, specialist expertise on a dedicated program, with the flexibility to expand across sponsors and therapeutic areas as your career progresses - and the security of a long-term IQVIA career even as individual programs evolve. \ N Through our long-standingpartnerships with the world's leading pharmaceutical and biotechnology companies, you'll contribute to clinical research programs that bring innovative treatments to patients worldwide, working across all phases of development and a broad range of therapeutic areas, within a culture that supports flexibility, continuous learning, and wellbeing. \ N \n Key responsibilities \ N \n Conduct site qualification, initiation, monitoring, and close-out visits in accordance with study protocols, GCP, ICH guidelines, and applicable regulatory requirements. \ N \n \n Ensure investigational sites maintain high standards of patient safety, data integrity, protocol compliance, and study quality. \ N \n \n Build and maintain effective relationships with investigators and site personnel, providing ongoing guidance, training, and support throughout the study lifecycle. \ N \n \n Monitor study progress, including regulatory documentation, patient recruitment and enrollment, data query resolution, and site performance metrics. \ N \n \n Collaborate with sites to implement and optimize patient recruitment and retention strategies to support study timelines. \ N \n \n Maintain accurate, complete, and inspection-ready study documentation, including Investigator Site Files (ISF), Trial Master Files (TMF), monitoring reports, and follow-up communications. \ N \n \n Identify, assess, and appropriately escalate study risks, site issues, and quality concerns while driving timely resolution. \ N \n \n Partner closely with cross-functional study teams to support successful study execution and delivery of project objectives. \ N \n \n Mentor andsupport junior clinical team members through coaching, training, and co-monitoring activities, as applicable. \ N \n \n Contributeto continuous improvement initiatives and support study start-up, maintenance, close-out, and site financial activities as required. \ N \n \n What you’ll bring \ N \n University degreein Life Sciences, Health Sciences, Nursing, Pharmacy, or a related discipline, or equivalent combination of education and experience. \ N \n \n 4 years minimum on-site monitoring experience of clinical trials within a CRO, pharmaceutical, biotechnology, or healthcare environment. \ N \n \n Strong knowledge of GCP, ICH guidelines, and applicable regulatory requirements. \ N \n \n Preferrable experience in a sponsor-dedicated or cFSP environment. \ N \n \n Knowledge of patient recruitment and study start-up activities is preferred. \ N \n \n Excellent communication, organizational, and stakeholder management skills. \ N \n \n Ability towork independently, manage multiple priorities, and collaborate effectively within cross-functional teams. \ N \n \n Willingness to travel within the assigned region (up to 40-60% of working time). \ N \n \n Please note this position cannot offer visa sponsorship, candidates must hold right to work in UK