Clinical Research Associate II - Job OverviewWhen our values align, there's no limit to what we can achieve. At Parexel, we all share the same goal - to improve the world's health. Fromclinicaltrials to regulatory, consulting, and market access, everyclinicaldevelopment is crucial.
About CTI: CTIClinicalTrial and Consulting Services is a global, privately held, full-serviceclinicalcontractresearchorganization (CRO) focused on the advancement of treatments for chronically and critically ill patient populations. We assistclinicalresearchthroughout the lifecycle of development.
Job Title:ClinicalResearchAssociate II
Job Location: Homebased, Brazil
Job Description: TheClinicalResearchAssociate II monitors investigational sites to ensure subject safety and provides high quality data review and reporting in compliance with the Caidya and/or client standards.
Responsibilities:
Track essential documents and report safety reports.
Ensure collation and distribution of study tools and documents.
Updateclinicaltrial databases (CTMS) and trackers.
Manage labeling requirements and coordinate/sign translation.
The SeniorClinicalResearchAssociate (Sr. CRA) is responsible for the delivery ofclinicalstudies at allocated sites and plays a key role in the local study team(s). Collaborating closely with Project ManagementClinicalOperations (PMCO) and Study Start-Up (SSU) manager.
By continuing, I agree to Recruit.net's Terms of Service. I also agree to receive email job alerts, to which I can unsubscribe at any time.#J-18808-Ljbffr