Executive: Clinical Research Associate II/Clinical Site Manager II - West - - (Boston, MA)

PAREXEL provides monitors with world class technology, training resources, and limited protocol load. You will also be rewarded for your hard work through our CRA bonus incentive program and career advancement opportunities. Your Key Accountabilities: Perform all clinical monitoring/site management activities for assigned projects in accordance with PAREXEL's standard operating procedures Act as PAREXEL's direct contact with assigned clinical sites, and use judgment to assess and ensure overall integrity of study implementation, as well as adherence to study protocol Conduct qualification visits (QV), site initiation visits (SIV) and monitoring visits (MV) at assigned clinical sites Thorough knowledge of applicable clinical research regulatory qualifications; i.e., Good Clinical Practice (GCP) and International Conference on Harmonization (ICH) guidelines Function as a mentor and role model for other CRA teammates Manage clinical monitoring activities