Phase I vaccine experience preferredfast paced studies10 site visits a monthThe Senior CRA will monitor the progress of clinical studies at investigative sites or remotely, and ensure clinical trials are conducted, recorded, and reported in accordance with the protocol, standard operating procedures (SOPs), ICH-GCP, and all applicable regulatory requirements.Responsibilities :Applies knowledge of ICONs policies and proceduresDemonstrates excellent written and oral communicationDemonstrates excellent knowledge of ICH / GCPDisplays ability to manage investigative sites to facilitate trial deliverablesDemonstrates ability to escalate issues appropriatelyConducts monitoring to confirm subject safety and data integrityDescribes and demonstrates the principals of IP accountabilityIdentifies scientific misconduct at the site levelDemonstrates working knowledge of Microsoft Office applications, Clinical Trial Management Systems, IVRS / IWRS and Electronic Data Capture platformsMentors CRAs new to the position or companyServes as an observation visit leaderConducts monitoring evaluation visitsAssists team lead in the development of trial tools or documentsAssists with CTM tasksParticipates in the development of process changes / improvementsPresents at client meetings / Investigator meetingsProvides training to trial teamsAt ICON, inclusion & belonging are fundamental to our culture and values. Were dedicated to providing an inclusive and accessible environment for all candidates. ICON is committed to providing a workplace free of discrimination and harassment. All qualified applicants will receive equal consideration for employment without regard to race, color, religion, sex, sexual orientation, gender identity, national origin, disability or protected veteran status.