JHU EEHPC este Laboratorul de Calcul de Înaltă Performanță Eficient Energetic al Universității Johns Hopkins, condus de Tinoosh Mohsenin. Laboratorul dezvoltă tehnologii medicale, pentru sănătate și portabile, concentrându-se pe calcul compact și eficient energetic pentru sisteme portabile și mobile. Cercetarea sa acoperă algoritmi, arhitectura calculatoarelor, componente hardware și integrarea sistemelor, combinând calculul de înaltă performanță cu inteligența artificială pentru aplicații precum monitorizarea inteligentă a sănătății, robotica și navigația autonomă. Activitatea laboratorului conectează cercetarea avansată în domeniul calculului cu provocări practice din sănătate, transport și utilități publice.
Senior Neurology Clinical Trial Compliance Monitoring Specialist (Remote, Maryland)
Lead risk-based remote compliance monitoring for multicenter neurology clinical trials. Safeguard GCP adherence, data integrity, regulatory accuracy, and site quality across study lifecycles.
Statele Unite ale Americii
Maryland57.195 $ – 100.040 $ / an
RemoteNormă întreagăSeniorLimbă Obligatorie: englezăConformitateDescriere
- Lead compliance monitoring for predominantly large, multicenter clinical trials managed by the BIOS Clinical Trials Coordinating Center
- Protect clinical trial data quality, accuracy, and integrity across study lifecycles through risk-based remote monitoring
- Partner with clinical trial teams nationwide
- Monitor trial metrics, protocol adherence, and required local, institutional, and federal regulatory compliance
- Track regulatory submissions, participant recruitment, CRF completion, and data-query resolution
- Assess new studies for quality assurance and content during risk assessments
- Create standard, protocol-specific, and trial-specific forms and monitoring plans
- Gather essential documents, maintain them, and submit them to the Trial Master File
- Train new research personnel in research compliance and deliver presentations
- Issue queries, follow up on noncompliance, prepare monitoring summaries, and communicate findings to investigators, research staff, and the Safety Monitoring Committee
- Review informed consent forms, source documents, trial records, and CRFs for accuracy, completeness, legibility, and consistency
- Report protocol, SOP, GCP, and regulatory deviations and implement appropriate corrective measures
- Assess whether adverse events are reported within required timeframes
- Arrange compliance monitoring visits and assess site procedures and GCP adherence
- Escalate quality concerns and support corrective-action efforts
- Support study teams preparing for external audits and participate in internal reviews at affiliate institutions when needed
- Educate investigators, clinical sites, and coordinators about remote monitoring and remote data entry
- Travel occasionally for monitoring visits
Cerințe
- Bachelor’s degree
- Five years of related clinical trial or medical research experience
- Thorough understanding of ICH GCP and FDA guidelines
- Experience with electronic data capture systems
- Exceptional attention to detail when reviewing clinical trial data, source documents, and regulatory compliance
- Additional education may replace required experience, and additional related experience may replace education beyond a high school diploma or equivalent, subject to the JHU equivalency formula
- Preferred: Bachelor’s degree in life sciences, health care, or a related field
- Preferred: Certification in human subjects research
- Preferred: Certified Clinical Research Associate (CCRA) credential
- Preferred: Experience in quality assurance, clinical trial auditing or monitoring, and/or good clinical practice
- Preferred: Experience with REDCap, SharePoint, and eIRB systems
- Intermediate proficiency in clinical documentation review
- Intermediate proficiency in data analysis
- Intermediate proficiency in documentation
- Intermediate proficiency in project management
- Intermediate proficiency in regulatory compliance
- Intermediate proficiency in SOP development
- Intermediate proficiency in training and development
Beneficii
- Total rewards package covering health, life, career, and retirement support
- Seasonal influenza vaccination required by Johns Hopkins University, with religious and medical exemptions available
- Required vaccinations for applicable roles are provided at no cost through Occupational Health
- Pre-employment accommodations are available
- Equal opportunity employment
- Background checks assess justice-involved backgrounds individually