- 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
- 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
- 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
- System One (Brentwood, TN)
- …abstraction from diverse sources * Obtain source documentation for patients enrolled into clinical trials and data registry * Maintain Data Registry as directed ... Title: Clinical Data Coordinator Location: Brentwood, TN...deadlines * Obtain source documentation for patients enrolled into clinical trial * Assist Clinical … more
- Georgetown Univerisity (Washington, DC)
- …is responsible for data management for phase I, II, and III oncology clinical trials conducted in the Lombardi Comprehensive Cancer Center (LCCC). Additional ... aspects of clinical research data management for clinical trials conducted in the LCCC ...varying complexity and disease indication. + Work collaboratively with trial stakeholders and internal study teams (physicians, Regulatory… more
- Sam Houston State University (Huntsville, TX)
- …is required; a Master's degree is preferred. Minimum of five years of experience in clinical research coordination or clinical trials administration or in a ... medical setting, with familiarity in informed consent, data collection, and regulatory compliance. Medical Assistant certification or relevant clinical … more
- Dartmouth Health (Lebanon, NH)
- …designee. * Primarily supports subject management, such as data entry in the Clinical Trial Management System(CTMS), scanning informed consents into EMR, and ... Carole Young Center for Digestive Health is seeking a Clinical Research Coordinator II to join our...* Site and Study Management * Organizes and manages clinical trials and research studies. * Conducts… more
- University of Miami (Miami, FL)
- … research and regulatory professional positions. CRS is Sylvester's centralized clinical trial office, supporting cutting edge Phase 1-3 oncology clinical ... trials for its catchment area. We provide administrative, regulatory , clinical , laboratory, quality, and training services to investigators at the medical… more
- Johns Hopkins University (Baltimore, MD)
- …a **_Research Program Coordinator (RPC)_** to coordinate assigned clinical trials , enrolled participants, and administratively manage protocol ... Participates in all mandatory meetings to develop increasing knowledge of assigned clinical trial requirements. + Participates in outreach, advertising, and… more