-development products, including setup, execution, and monitoring. Ensure adherence to study protocols and timelines. Collect... documentation of study activities, including test plans and results, subject information, and protocol deviations. Communicate...
The Sr. Mgr., Clinical Study Inspection Readiness, is responsible for leading clinical inspection readiness activities... to support the Program Operations Leader and Clinical Study Lead(s) for one or more assigned clinical programs within Clinical...
on site, part-time working off-site) Position Summary The Clinical Study Coordinator will coordinate clinical research... team and a diverse research team to meet project goals. The Clinical Study Coordinator will be independent, responsible...
Purpose As TMF Study Owner you will ensure that the clinical trial documentation must be consistent with the Trial... and other requirements. The TMF Study Owner (SO) is the subject matter expert to and single point of contact for the Project Manager (PM...
timelines and foster relationships with approximately 100 study sites across the United States, ensuring seamless communication... and collaboration. Provide comprehensive support to study sites by responding to emails and phone inquiries within 24 hours...
projects of varying sizes Troubleshoots hardware and software challenges, analyzes engineering data to make study-level... status with keen focus on data quality and schedule Develop study documents like consent forms, statements of work, and SOPs...
Position Summary The Institute for Global Health in the College of Osteopathic Medicine seeks a Study Abroad... coordinator to aid the unit facilitating the preparation of Study Abroad programs for IGH with OEA and in-country logistics. The...
As a Senior Clinical Study Lead (SCSL), you will lead the cross-functional study team responsible for the global... execution of large, complex clinical trials from study design through study close out. These responsibilities...
. Requires study coordinator experience or experience in oncology clinical trials. Ability to work on evenings, weekends... medical records and data extraction. SOCRA/ACRP Certification Study coordinator experience and experience in oncology...
across business units and develop plans to achieve objectives. Approve the Study Startup, Study Monitoring and protocol recruitment... plans. Resolve escalated issues identified by the site activation sub team in partnership with the Study Operations Manager...