... at site (trial personnel including study coordinators, pharmacists, etc.) Qualifications Needed: ... to meet all of our study timelines Ability to operate and ... influencing skills to effectively manage study sites both remotely and face ...
... at site (trial personnel including study coordinators, pharmacists, etc.) What do ... to meet all of our study timelines Ability to operate and ... influencing skills to effectively manage study sites both remotely and face ...
... home office based sleep studies through the use of appropriate ... transport (if undertaking ward studies) Must be available to work ... patients with sleep study set ups remotely via video ... to facilitate the sleep study reporting as requested by physicians ...
... : Responsible for activation of all study sites to meet project timelines ... Identify quality issues within the study to implement appropriate corrective action ...
... managing, implementing and monitoring clinical studies, with support, in a team ... collection and review throughout the study lifecycle inclusive site activation. Manage ...
... trial with adequate site study supplies (such as Non - IP, ... for communication with the study teams and sites. Candidates must ... meet all of our study timelines Ability to operate and ... skills to effectively manage study sites both remotely and face ...
... clinical data and that the study is conducted in compliance with ... , during, and after a clinical study; assists with resolution of investigational ... assignments in support of additional studies or departmental initiatives. May serve ...
... contact and build relationships with study investigators sites and networks in ... conduct of feasibility and potential study participation. • To perform phone selection ... with other departments such as Study Start Up, CRA management to ...
... assigned regional clinical study leadership and or global clinical study leadership of smaller studies and or vendor set-up ... Pharma with global studies Holds more than 5 solid years of CRA with global oncology studies What ICON can offer you: ...
... in conjunction with study team. Perform initial review of CRO and other third party study vendor invoices to ensure that ... trials teams; include the study team meetings. Function as the ... from initiation to clinical study report). Used to work in ...