• Thousand Oaks, CA, USA
May 25, 2022  
Primary Responsibilities: Participate in study-specific meetings such as study team meetings, vendor meetings, investigator meetings. Contribute to sponsor oversight of clinical monitoring activities (e.g., may review monitoring visit reports, monitoring plans, etc.) to ensure completion of appropriate resolution of site-related issues, including any necessary site or study level corrective action plans. Support cross-functional study team meetings (e.g., distribute agenda, take minutes, document action items & decisions), and follow up with responsible functions on study team deliverables. Prepare/review study-related documents (e.g., ICF template, CRFs, Laboratory Manual, CRF Completion Guidelines) and site-related documents (e.g., site-specific informed consent, study tools/worksheets, investigator contracts, site budget). Assist with development of clinical trial communications (e.g., newsletters) for sites....
CodeForce360 Thousand Oaks, CA, United States