- IQVIA (Lilburn, GA)
- …This individual will play a key role in assisting in the conduct of clinical trial activities, in accordance with all applicable regulations governing the ... conduct of clinical trials . The primary skills include logical...as required + May be asked to perform special project responsibilities and travel to other CCT locations when… more
- Sumitomo Pharma (Atlanta, GA)
- …supply management, data management, IT, and external vendors. + Work with the Clinical Project Team to define user role-based training for internal/external ... release, vendor governance, change control, and data integration/reconciliation. The manager ensures randomization, treatment assignment, and clinical -supply… more
- University of Miami (Miami, FL)
- …colleagues and stakeholders. Department Specific Functions We are seeking a mission-driven Sr. Project Coordinator - Project Manager to support a ... has an exciting opportunity for a Full Time Sr. Project Coordinator to work at the UHealth medical campus...implementation of digital tools and web applications that support clinical trials , participant engagement, and data capture.… more
- BD (Becton, Dickinson and Company) (San Diego, CA)
- …prepares publication and dissemination strategy, and ensures clinical trial excellence including study protocol development, evidence project execution, ... **Job Description Summary** As Manager , Medical Affairs, you will be responsible for...Medical Affairs, you will be responsible for both the clinical and administrative aspects of MMS business. This includes… more
- Bristol Myers Squibb (Madison, NJ)
- …effective risk and issue management. Provide quality and compliance consultation to clinical trials teams throughout study lifecycle and establish a feedback ... adjusted when new or unanticipated issues arise once the trial has begun. **Key Responsibilities:** + Develop the Quality...deemed necessary. + Provide quality and compliance consultation to clinical trials teams throughout study lifecycle. +… more
- Johns Hopkins University (Baltimore, MD)
- …patient flow. + Develops and maintains protocols for study. Develops consent forms for clinical trials from protocols. Prepare materials for IRB such as Change ... oversee and maintain multiple complex studies. The Sr. Research Project Coordinator oversees the day-to-day activities of a single...and reports, as needed. + In conjunction with the Clinical Research Manager , trains new study staff… more
- HCA Healthcare (Nashville, TN)
- …to consult with leadership. + Proficiency required in interpreting drug literature and clinical trial evaluation + Ability to reason and translate clinical ... invests in you as a Senior Pharmacy Benefit Account Manager ? At HealthTrust, you come first. HCA Healthcare has...relationships with key internal Account Directors and Managers, and Clinical Resources within HealthTrust to become a trusted advisor… more
- Georgetown Univerisity (Washington, DC)
- …The Research Data Manger will be responsible for managing data for a portfolio of clinical trials overseen by the Clinical Research Organization (CRO) at ... clinical departments within GUMC, and the Research Data Manager plays a critical role in ensuring that all...integrity of clinical research data for non-oncology clinical trials . This position is responsible for… more
- University of Pennsylvania (Philadelphia, PA)
- …individual to support the fast-paced day-to-day operations of multiple clinical trials , investigator-initiated studies, and translational biobank projects ... alongside a team of study coordinators, a regulatory specialist, project managers, investigators, and clinical staff to...strategies for participant recruitment. * Work closely with the Clinical Research Program Manager on study start-up… more
- Bristol Myers Squibb (San Diego, CA)
- …regulatory authority interactions, design, and execution of Phase 0 to Phase 3 clinical trials , and medical monitoring. This role provides medical direction and ... clinical study reports, and review of other clinical trial and regulatory documents + Conduct...and Independent Data Monitoring Committees as applicable + Conduct clinical trials using ethical guidelines relevant to… more