About the Role
RBW Consulting are excited to announce an opportunity on behalf of one of our close clients. This company are a renowned CRO with leading healthcare intelligence and a European culture. They treat unmet disease target areas and advance clinical research by providing outsourced services to pharmaceutical and biotechnology companies. Key accountabilities Autonomy of investigator sites with full responsibility for the successful management of sites through study life cycle (start-up to close-out); Conduct feasibility, pre-study, initiation, monitoring, and closeout visits for research sites, mainly phase 1 to 3 and within all available therapeutic areas; Prepare accordingly and attend investigator meetings, coordinating timely delivery and subsequent proper storage and accountability of clinical supplies and following-up of drug safety issues; Perform source document verification and case report form review; Perform regulatory document review; Conduct study drug inventory; Perform adverse event and serious adverse event reporting and follow-up; and Assess patient recruitment and retention. Qualifications Bachelor of Science in health-related field (or equivalent) Proven CRA experience; 6 years minimum Broad knowledge of medical terminology and clinical patient management Basic knowledge of drug therapy techniques and clinical research methodologies To apply: Please click ‘apply’ or contact Harry Henson for any further information.