Clinical Research Site Start Up Specialist (Raritan, IL)

Clinical Research Site Start Up Specialist

s www.globalchannelmanagement.com jobopeningsjobs(at)globalchannelmanagement.co m Clinical Research Site Start Up Specialist needs 3-5 years experience in clinical researchClinical Research Site Start Up Specialist requires prior experience as Study Start-Up Specialist but not mandatory Knowledge Skills and Abilities Knowledge of FDA regulations required. Advanced skills in Microsoft Word Microsoft PowerPoint Microsoft Excel Microsoft Outlook Experience with Adobe Acrobat Professional and Microsoft Access a plus Must possess excellent skill ability in the following Clinical Research Site Start Up Specialist needs execute study start-up for assigned protocols with the goal of meeting study start-up timelines. Monitor project plans to meet Site Initiation Readiness at the Investigator Meeting. Ensure the accuracy and quality of deliverables from clinical team and vendors. Maintain project metrics and provide status updates to senior management. Manage information sharing (i.e. Site Start-Up tracker Site Identification Tracking Tools). Develop Standard Operating Procedures and Working Documents to document and communicate unit s processes and procedures. Actively share new ideas for efficient and seamless processes during study team meetings. Aggressively seek input from other departments on process improvement and implements process improvement for Site Start-Up initiatives. Provide agendas meeting minutes and manages follow up items for all Site Start-Up meetings that are assigned.