* Represent PPD in the global medical research community and develop and maintaincollaborative relationships with investigational sites and client company personnel.* May assist project manager or clinical team manager on assigned projects.* Continue to complete CRA II responsibilities as defined below.CRA II: * Represented PPD in the global medical research community and developed and maintaincollaborative relationships with investigational sites. * Continued to… Show more * Represent PPD in the global medical research community and develop and maintaincollaborative relationships with investigational sites and client company personnel.* May assist project manager or clinical team manager on assigned projects.* Continue to complete CRA II responsibilities as defined below.CRA II: * Represented PPD in the global medical research community and developed and maintaincollaborative relationships with investigational sites. * Continued to complete CRA I responsibilities as defined below. CRA I: * Performed and coordinated all aspects of the clinical monitoring and site managementprocess in accordance with ICH GCP, FDA guidelines, local regulations and PPD SOPs. * Conducted site visits to assess protocol and regulatory compliance and manages requireddocumentation.* Responsible for ensuring that data will pass international quality assurance audits. * Developed collaborative relationships with investigational sites.CRA I-O:* Supporting in house activities * Collecting regulatory documents* Preparing files for regulatory authorities* Trackers updates* Preparing Initiation visits and close out visit * Documents shipments Show less