Deb O Email and Phone Number

Prepare and conduct site visits including (but not limited to): qualification visits, initiation visits, monitoring visits, motivational visits, audit support visits and close-out visits according to relevant SOPs, local requirements, the protocol and project plans as well as providing timely and comprehensive visit and status (i.e. patient recruitment) reports· Communicatew effectively with Project Team members (i.e. Clinical Team Leader, Project Managers, Safety and Data Management) to ensure study completion per company and client requirements and timelines· Being a proactive member in team calls and act as a role model· May support in the creation of CRA working tools based on the experience on the project· Proactively communicate with study sites and follow-up on all open issues in order to meet the project timelines· Ensure that all study-related documentation is tracked, printed and filed as required by Chiltern SOPs, regulatory requirements and other protocols· To ensure that investigator site files are assembled appropriately and that all required documentation is in place, tracked and reconciled on a regular basis against the TMF files· May support in mentoring less experienced CRAs on project or department tasks and requirements.