Under general supervision the Clinical Research Quality Assurance Specialist II is responsible for the oversight of clinical research study protocols of increasing complexity, with an emphasis on quality, training, monitoring, and the development of tools for study team use. The Clinical Research Qu...
Under general supervision the Clinical Research Quality Assurance Specialist II is responsible for the oversight of clinical research study protocols of increasing complexity, with an emphasis on quality, training, monitoring, and the development of tools for study team use. The Clinical Research Qu...
Enhance your career at raSmith as a Land Survey Project Manager in our Survey Services division and discover why we're ranked #2 as a Top Workplace. Land Survey Project Manager - Wisconsin Market - Primary Responsibilities:. Assessing project requirements and developing a sound approach to meet the ...
Coordinate the day-to-day administrative activities of a health-disparities/health equity focused clinical research and health improvement program. Coordinate research protocols including arranging necessary appointments and procedures, working collaboratively with other departments and institutions...
Clinical Research Assistant II. Accurately enter research data onto case report forms or specified programs (OnCore) and other databases as appropriate under the direction of the research nurse or study coordinator. Collect required data from study coordinators and research nurses, and enter onto cl...
Perform the day-to-day administrative activities of the clinical research trials program. Coordinate research protocols including arranging necessary appointments and procedures, working collaboratively with other departments and institutions, and maintaining contact with study participants. Identif...
Under the direction of the research principal investigator and manager, the Clinical Research Assistant III works collaboratively to support hematology, oncology, bone marrow transplant, and cellular therapy clinical trials for pediatric patients. Provide support as needed to back up clinical resear...
Develop and maintain project schedules, budgets, and resource plans to ensure successful project execution. This role requires a proactive individual who can manage complex projects, meet deadlines, and exceed customer expectations. Collaborate with cross-functional teams, including engineering, fin...
Clinical Research Assistant II. Function as a Program Assistant in the Center for Advancing Population Science (CAPS). Under the direction of the principal investigator, assist in enrolling patients in educational and social intervention research studies. Data Collection for Research Studies. ...
Coordinate the day-to-day administrative activities of the clinical research trials program, including mentoring Research Regulatory Specialists with a focus on study activation. Advise CTO Research Managers, Research Nurses, and Research Coordinators to identify, prioritize, and complete all regula...
Develop, plan and implement experiments, analyze data and compile results, monitor quality control processes to ensure integrity of research, and prepare and write manuscripts and grant applications. Coordinate research study activities; lead and manage projects. Participate in meetings with princip...
Perform the day-to-day administrative activities of clinical research trial programs. Project/patient coordination for research protocols including arranging necessary appointments and procedures, working collaboratively with other departments and institutions, and maintaining contact with study par...
The Statistical Research Scientist will be involved in every aspect of the research enterprise, including study design and consultation with basic scientists and clinicians, data management, analysis, and preparation of progress report and manuscripts. The Statistical Research Scientist will support...
Clinical Research Coordinator II - GOOD Study. Perform the day-to-day administrative activities of clinical research trial programs. Coordinate research protocols including arranging necessary appointments and procedures, working collaboratively with other departments and institutions, and maintaini...
Provide support as needed to back up clinical research functions including patient enrollments, informed consents, and facilitate/coordinate clinical research activities designated by protocols and maintain appropriate clinical research data records. Under the direction of the research principal inv...
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