You will be supporting a long-term partnership with one of the most established pharmaceutical companies in the industry. Within this program, you will find a culture focused on teamwork and camaraderie, where every member plays an integral part. You will have the opportunity to work on breakthrough technologies in the areas of cardiovascular, oncology, women's health, and cell & gene therapy. This is a challenging career path that will support your growth and professional development.As a Clinical Research Associate, you will coordinate all aspects of the clinical monitoring and site management process in accordance with regulatory guidelines, local regulations, and standard operating procedures. In this role, you will be a decision maker, solving problems independently or as part of the client and ICON team. You will be managing competing priorities, supporting the on-site team, ensuring investigators follow the clinical trial protocol, providing training, and most importantly, motivating the team to ensure high-quality results.What you will be doing: You will monitor multiple Phase I, II, III & IV clinical trial sites across different therapeutic areas.Assist other CRAs with co-monitoring activities both remote and on-site.You will utilise your customer service mindset with your sites focusing on delivering value, building loyalty and trust to create a positive impact and strong relationship with investigators and study coordinators where respect, knowledge and commitment to ICH/GCP guidelines are key to successful trial conduct.As the CRA, you are the main sponsor representative, providing key project updates.You will collaborate with the team, developing commitment to study timelines and objectives through regular visits with site staff in-person and remotely.You will be the first to review 'source to CRF/eCRF,' ensuring patient safety and data integrity aspect of the study.As the first point of contact for study sites, escalating any concerns/issues to other departments including Safety, Investigational Medicinal Product, Local Study Managers, and management team as appropriate.Additionally, you will oversee the sites' adherence to GCP/ICH practices, ensuring quality of study conduct.You are: Bachelor's Degree with 2-4 years of relevant healthcare experience in the pharma or clinical research industry.Minimum 1 - 2 years of monitoring and site management experience.Working knowledge of Local Regulations.A demonstrated working knowledge of ICH/GCP Guidelines.Excellent record-keeping skills and attention to detail.Experience conducting Site Selection, Initiation, Routine Monitoring and Close Out Visits both remotely and on-site.Fluent in English, both written and oral.Strong technical skills with CTMS, eCRF, eTMF.Benefits of Working in ICON: Our success depends on the knowledge, capabilities, and quality of our people.#J-18808-Ljbffr
