- Vanderbilt University Medical Center (Nashville, TN)
- …monitoring efficient invoicing and taking appropriate action to maintain clinical trial billing compliance, providing reports investigators, department ... prior to, during and after the conduct of a clinical /translational trial . Participates in periodic site visits...protections for human participants of research and through ongoing monitoring of trial processes and participants *… more
- Vanderbilt University Medical Center (Nashville, TN)
- … coordinator will also be responsible for working with the overall study coordinator and Clinical Trials Manager to insure appropriate adherence to study ... trials, our research group currently has multiple funded behavioral clinical trials. As such, the coordinator will... will either be directly collecting the data or monitoring research staff who are collecting the data. +… more
- Vanderbilt University Medical Center (Nashville, TN)
- …monitoring efficient invoicing and taking appropriate action to maintain clinical trial billing compliance, providing reports investigators, department ... prior to, during and after the conduct of a clinical /translational trial . Participates in periodic site visits...protections for human participants of research and through ongoing monitoring of trial processes and participants *… more
- Vanderbilt University Medical Center (Nashville, TN)
- …study budgets, monitoring efficient invoicing and taking appropriate action to maintain clinical trial billing compliance * Serves as an advocate for human ... prior to, during and after the conduct of a clinical /translational trial . Participates in periodic site visits...protections for human participants of research and through ongoing monitoring of trial processes and participants *… more
- System One (Nashville, TN)
- …Duties include but are not limited to: * Supports enrolling patients onto the clinical trial through screening, enrollment and follow up of eligible subjects ... Position: Clinical Research Coordinator Location: Nashville, TN-...enroll and follow study subjects ensuring protocol compliance and monitoring while the subjects are on study. Responsible for… more
- Edwards Lifesciences (Nashville, TN)
- …exam results for consistency with case report form, and determine if clinical trial /study subject documentation is within parameters of study hypothesis, ... as well as to monitor clinical trial /study safety, in keeping with protocols,...+ Clinical research certification (ACRP or SOCRA, Clinical Coordinator /CRA certification) + Prior clinical… more
- J&J Family of Companies (Nashville, TN)
- …of documentation needed for internal and external audits to ensure all essential clinical Trial Master File (TMF) documents are compliant with Good Documentation ... parameters of study hypothesis, as well as to monitor clinical trial /study safety, in keeping with protocols,...+ Clinical research certification (ACRP or SoCRA, Clinical Coordinator /CRA certification) **Other:** + Must upload… more
- Vanderbilt University Medical Center (Nashville, TN)
- …Summary:** JOB SUMMARY The department of Pediatric Hematology-Oncology is seeking a Clinical /Translational Research Coordinator III to join our research team. ... prior to, during and after the conduct of a clinical /translational trial . Participates in periodic site visits...protections for human participants of research and through ongoing monitoring of trial processes and participants. With… more
- Merck (Nashville, TN)
- …The CQOM will oversee headquarters clinical quality operations and support clinical trial teams within the assigned therapeutic area, to proactively embed ... Categorization Tools and Quality Plans in partnership with the Clinical Trial Team (CTT). + Collectively and...include, but not be limited to: 1) Facilitating and monitoring CTT oversight of vendors; 2) Development, review and… more
- Vanderbilt University Medical Center (Nashville, TN)
- …Pediatric Gastroenterology **Job Summary:** JOB SUMMARY The Clin/Tran Research Coordinator I will manage, independently or with general direction, the ... gastrointestinal conditions in children and adults. . The Research Coordinator will be responsible for coordinating the approval processes... will either be directly collecting the data or monitoring research staff who are collecting the data. +… more