- Johns Hopkins University (Baltimore, MD)
- …maintenance and accuracy of all clinical research data for complex and detailed clinical trials and may assist with orientation of less senior research staff ... information. This is an intermediate level position in managing clinical trials and/or registry databases within the...all mandatory meetings to develop increasing knowledge of assigned clinical trial and Registry requirements. + Will… more
- McLaren Health Care (Detroit, MI)
- …study coordinator /data management/ regulatory specialist support to the Clinical Trials Office (CTO). Manage independent assignment, providing excellent ... customer support and guidance in the clinical trials arena. **Responsibilities:** + Assure all studyrequirements are met and documented and meet both internal… more
- McLaren Health Care (Detroit, MI)
- …study coordinator /data management/ regulatory specialist support to the Clinical Trials Office (CTO). Manage independent assignment, providing excellent ... customer support and guidance in the clinical trials arena. **This position is onsite in Detroit, Michigan.** **Responsibilities:** + Assure all study… more
- Stanford University (Stanford, CA)
- Assistant Clinical Research Coordinator (Hybrid Opportunity) **Stanford, California, United States** **New** Research Post Date 2 days ago Requisition # 106973 ... Stanford University is seeking anAssistant Clinical ResearchCoordinator at 100% FTEto perform administrative support duties related to the collection of clinical … more
- University of Miami (Miami, FL)
- …studies. This will include all aspects of coordinating a clinical research trial in terms of regulatory reporting, assisting with medication dispensing from ... of Medicine has an exciting opportunity for a full-time Clinical Research Coordinator 2 to work on...expected to meet with study monitors and maintain all regulatory documents. Hours may fluctuate depending on clinic and… more
- Mount Sinai Health System (New York, NY)
- …the preparation of new protocol submissions, protocol amendments, and renewals of ongoing clinical trials . 6. Obtains informed consent under supervision of the ... Principal Investigator, Clinical Research Manager, or Senior Clinical Research Coordinator for studies enrolling vulnerable subjects, and for studies… more
- Emory Healthcare/Emory University (Atlanta, GA)
- … II handles administrative activities generally associated with the conduct of clinical trials . KEY RESPONSIBILITIES: + Manages research project databases, ... with source documents, attends monitoring meetings with sponsors. + Prepares regulatory submissions. + With appropriate credentialing and training may perform… more
- Emory Healthcare/Emory University (Atlanta, GA)
- …assists with the administrative activities generally associated with the conduct of clinical trials . KEY RESPONSIBILITIES: + Maintains data pertaining to ... physicians, therapists, and psychologists in observational and interventional patient-based clinical research related to pre-term infants and young children with… more
- McLaren Health Care (Bay City, MI)
- …data on potential candidates, verifying appropriateness of patients for entry to clinical trials , and assisting the other staff in determining eligibility ... the investigators and clinicians in identifying and enrolling eligible patients into clinical trials / studies and assures compliance to protocol requirements. 8.… more
- Emory Healthcare/Emory University (Atlanta, GA)
- …assists with the administrative activities generally associated with the conduct of clinical trials . KEY RESPONSIBILITIES: + Maintains data pertaining to ... and monitors charges. + Assists with quality assurance and tracks regulatory submissions. + Performs related approved responsibilities as required. MINIMUM… more