- Arkansas Children's (Little Rock, AR)
- …The Clinical Research Professional I coordinates selected specific aspects of clinical research studies . This role serves as a resource for research study ... members of the clinical research team regarding specified aspects of the study . **Additional Information:** **Required Education:** High school diploma or GED or… more
- AT Still University (Mesa, AZ)
- …+ Lead, plan, implement, and execute research projects to successfully meet research study objectives. + Lead and assist with a variety of research program events. ... other key stakeholders (eg, research team members, funders, regulatory bodies) on study -specific research processes. + Research study data collection planning,… more
- University of Southern California (San Diego, CA)
- …with research teams and community partners to ensure outreach efforts engage the study populations of interest and align with ATRI's mission to advance Alzheimer's ... and related dementias research through equitable study participation. Key Responsibilities: + Develop and execute outreach strategies that promote representative… more
- Taiho Oncology (Pleasanton, CA)
- …of key tasks involved in the design, conduct, monitoring and review of study data, analysis and reporting of clinical trials. Performance Objectives: + Collaborates ... the creation of relevant high-quality clinical documents such as study protocols and clinical study reports (CSRs),...and leverages the knowledge for designing and summarizing clinical studies . + Keeps Sr. Medical Director current on status… more
- University of Miami (Miami, FL)
- …procedures according to the protocol. + Coordinate routine activities of clinical studies including data collection and maintenance, planning study timelines, ... CORE JOB FUNCTIONS + Perform chart review/pre-screening activities for study participant eligibility and coordination of simple clinical research protocols.… 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 RESPONSIBILITIES: + Performs chart review/pre-screening activities for study participant eligibility and coordination of simple clinical research… more
- Mount Sinai Health System (New York, NY)
- …trauma and early brain-behavior development. The research team will recruit and study participants in a longitudinal prenatal cohort design (ie, beginning in ... Psychiatry and Ob/Gyn. Responsibilities include participant recruitment and enrollment, scheduling study visits, conducting study visits (pregnancy and mental… more
- J&J Family of Companies (Irvine, CA)
- …manage company sponsored clinical trials, ensuring compliance with timelines and study milestones. + Oversees/executes feasibility, selection, set up, conduct and ... trial sites (eg site management); + Develops clinical trial documents (eg study protocol, informed consents, CRF, monitoring plan, study manual, investigator… more
- Cedars-Sinai (Los Angeles, CA)
- …Program Administrator, or Research Nurse to coordinate and/or implement the study . Evaluates and abstracts research data and ensures compliance with protocol ... the IRB. Provides limited patient contact as needed for study and assist with study budget and...Category** : Academic / Research **Job Specialty** : Research Studies / Clin Trial **Overtime Status** : NONEXEMPT **Primary Shift**… more
- Rush University Medical Center (Chicago, IL)
- …research teams. Under close supervision, the CRA assists with essential study tasks such as organizing regulatory files, entering participant information, preparing ... materials for study visits, and observing study procedures for...for training. This role supports minimal to moderate risk studies , including exempt or expedited protocols, and is not… more
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