Monitor clinical trial sites in Germany for CTI, serving as their primary contact and supporting study visits, documentation, investigational products, and remote monitoring.
Monitor clinical trials across China for ICON, supporting protocol compliance, reliable data, and patient safety. Work with investigators and site teams throughout each study.
Lead clinical data management delivery for EDETEK’s CONFORM eClinical implementations and clinical trial projects. Oversee client coordination, user acceptance testing, documentation, and development of junior team members.
संयुक्त राज्य
पेंसिल्वेनियाCoordinate participant recruitment, study visits, regulatory submissions, and data management for clinical research at the University of Pennsylvania. Support clinical investigations at Penn’s Perelman School of Medicine.
Support AbbVie oncology trials in China by monitoring clinical sites, managing study risks and helping protect compliance, recruitment and data quality.
Monitor sponsor-dedicated clinical trials for ICON and coordinate study setup, documentation, compliance, and investigator relationships. Based in São Paulo, Brazil, this remote role supports clinical research operations.
संयुक्त राज्यपेंसिल्वेनियाCoordinate participant visits, informed consent, data collection, and IRB compliance for University of Pennsylvania clinical studies. Support research activities at study sites in Philadelphia.
Lead early-phase clinical research advancing medicines for Alzheimer’s, Parkinson’s, ALS, and other neurodegenerative diseases. Shape trial design, analyze evidence, and support regulatory development.
संयुक्त राज्य
कैलिफ़ोर्निया
कोलोराडो
मिनेसोटाOversee clinical sites, study documentation, and data quality for Medtronic neurovascular device studies. Coordinate compliant study delivery with investigators, vendors, monitors, and internal teams.
संयुक्त राज्य
मैरीलैंड
वर्जीनियारिमोटपूर्णकालिकजूनियरमध्य स्तरडिग्री आवश्यक नहींआवश्यक भाषा: अंग्रेज़ीनैदानिक अनुसंधानMonitor oncology clinical trial sites for Parexel, a provider of clinical development, regulatory, consulting, and market access services. Oversee site compliance, participant safety and recruitment, and study documentation.
Oversee investigator sites and monitor clinical trials for Parexel, supporting patient safety, GCP compliance, recruitment, and study quality. The role covers sites across the United States and is listed as remote in Arizona.
संयुक्त राज्यकैलिफ़ोर्नियाकोलोराडोमिनेसोटाOversee clinical study sites, data quality, and regulatory records for Medtronic’s neurovascular technologies. Support compliant studies from site activation through closeout.
संयुक्त राज्यकैलिफ़ोर्नियाSupport AbbVie’s neurology clinical trials by monitoring research sites and helping uphold regulatory compliance, data quality, patient safety, and recruitment goals.
संयुक्त राज्यपेंसिल्वेनियाCoordinate participant screening, study visits, data collection, and regulatory tasks for clinical research at the University of Pennsylvania Perelman School of Medicine.
संयुक्त राज्यपेंसिल्वेनियाCoordinate participant visits, study protocols, IRB submissions, and clinical data for the University of Pennsylvania’s medical research programs.
संयुक्त राज्य
विस्कॉन्सिनAnalyze industry-sponsored clinical trial data for UW–Madison’s Statistical Data Analysis Center. Support independent data monitoring committees with statistical methods, study design, and reporting.
