- Brown University (Providence, RI)
- …a full-time grant-funded Research Assistant to work on several different research studies relating to mental health in families and youth. The successful applicant ... will have a direct impact on the different research studies . Job-related activities include but are not limited to:...activities include but are not limited to: (1) conducting study -related formative research; and (2) recruiting study … more
- Houston Methodist (Houston, TX)
- …clinical research protocols, gathering patient data via methods specified in the study protocol, study reports. This position ensures accurate data collection, ... documentation organization, and safety of study volunteers. **FLSA STATUS** Exempt **QUALIFICATIONS** **EDUCATION** + Bachelor's degree in a related field +… more
- Houston Methodist (Houston, TX)
- …clinical research protocols, gathering patient data via methods specified in the study protocol, study reports. This position ensures accurate data collection, ... documentation organization, and safety of study volunteers. **FLSA STATUS** Exempt **QUALIFICATIONS** **EDUCATION** + Bachelor's degree in a related field +… more
- Houston Methodist (Houston, TX)
- …clinical trial activities and plays a critical role in the conduct of the study . This position functions at the Competent level according to the Benner's model of ... of the GCP compliance, financial and other related aspects of the research study . This position serves as a liaison between physicians, patients, staff and sponsors.… more
- University of Miami (Miami, FL)
- …procedures according to the protocol.2. Coordinates routine activities of clinical studies including data collection and maintenance, planning study timelines, ... timelines. CORE JOB FUNCTIONS1. Performs chart review/pre-screening activities for study participant eligibility and coordination of simple clinical research… more
- BeOne Medicines (San Mateo, CA)
- …is essential, including involvement in all stages of clinical trials (from start up to study report), ideally having taken at least one study through from start ... their existing skills to oncology. * Expert understanding of global clinical study design and drug development process from discovery to registration and… more
- Cedars-Sinai (Los Angeles, CA)
- …Description** The Clinical Research Coordinator I works independently providing study coordination, screening of potential patients for protocol eligibility, ... response to sponsor queries. Responsible for compiling and reporting on each study including information related to protocol activity, accrual data, workload, and… more
- University of Utah (Salt Lake City, UT)
- …as part of natural historystudies in ophthalmic diseases. Interact with clinical study sites and sponsors regarding organization of the reading center in close ... Utah: benefits.utah.edu** **Responsibilities** **Essential Functions:** + Interact with clinical study sites and the sponsors regarding organization ofreading center… more
- University of Miami (Miami, FL)
- …procedures according to the protocol. Coordinates routine activities of clinical studies including data collection and maintenance, planning study timelines, ... timelines. CORE JOB FUNCTIONS Performs chart review/pre-screening activities for study participant eligibility and coordination of simple clinical research… more
- IQVIA (Durham, NC)
- …Overview Perform monitoring and site management work to ensure that sites are conducting the study (ies) and reporting study data as required by the study ... with project needs to enhance predictability. * Administer protocol and related study training to assigned sites and establish regular lines of communication with… more
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