The CR Quality Specialist C is responsible for performing GCP compliance activities for sponsored IND clinical research trials and Investigator initiated trials to verify human subjects are safe, the data accurate, complete and verifiable from source documents. The Clinical Research Quality Speciali...
The Clinical Research Data Specialist supports the data collection, analysis and reporting functions for the Office of Clinical Research (OCR) for assigned oncology trials in Phase I, II or III clinical trials and works in conjunction with a Clinical Research Nurse/Coordinator (CRN/CRC) to ensure ac...
Minimum of seven years of experience as a clinical research monitor/auditor, research nurse or research coordinator with at least three years’ experience directly monitoring/auditing or five years’ experience preparing for and fully supporting monitoring/auditing visits preferred. Additional experie...
The ACC One Cancer Clinical Research (OCCR) is instrumental in the development and implementation of cancer clinical trials that offer cutting-edge oncology treatments. The ACC OCCR Regulatory Affairs Office seeks a full-time Regulatory Affairs Specialist-CC to participate in the coordination of Pha...
The ACC seeks a full-time NCI/NCTN Senior Regulatory Affairs Study Start-Up Specialist to participate in the coordination of Phase I-III clinical trials sponsored by the NCI/NCTN. The NCI/NCTN Senior Regulatory Affairs Start-Up Specialist is expected to resolve, with minimal supervision, regulatory ...
Minimum of seven years of experience as a clinical research monitor/auditor, research nurse or research coordinator with at least three years’ experience directly monitoring/auditing or five years’ experience preparing for and fully supporting monitoring/auditing visits preferred. Additional experie...
The CR Quality Specialist C is responsible for performing GCP compliance activities for sponsored IND clinical research trials and Investigator initiated trials to verify human subjects are safe, the data accurate, complete and verifiable from source documents. The Clinical Research Quality Speciali...
Substantial Site Management experience or equivalent experience in clinical research, with understanding of clinical trials methodology and terminology. Update all appropriate Clinical Trial Management Systems (CTMS) on an ongoing basis, including performing regular reviews of site level data in cli...
Initiation Clinical Research Associate. Previous experience in study set up / site initiation / study start up experience or equivalent experience in clinical research environment, with understanding of clinical trials methodology and terminology. ...
SOP(Standard Operating Procedure).SDV: Source Data Verification).IRB (Institutional Review Board)....
The RA III manages Research Assistants and Research Associates working on research and evaluation tasks including sampling, weighting, data management, statistical analysis, continuous quality improvement, reports and presentation. The Research Associate III (RA III) functions in a highly collaborat...
This position is responsible for fulfilling document delivery, and docket and case procurement requests using traditional and online sources (WorldCat, Lexis+, Westlaw, Bloomberg BNA, Internet, PACER, Courthouse News, and a variety of additional commercial and local providers), and other light legal...
Ensure that projects are completed on schedule following established procedures, schedules, and work plans. Coordinate the planning, organizing, control, integration, and completion of Engineering projects within area of assigned responsibility. ...
We are seeking a Project Coordinator who will play a crucial role in supporting the operations and initiatives of the CDMRP Dept of Defense Spinal Cord Injury Research Program funded research project Improving Cardiometabolic Health in Individuals with Spinal Cord Injury Using Home-Based Interactive...
The Clinical Resarch Coordinator is a research professional who ensures oversight and compliance of both system-wide and local clinical research activities. We have an opportunity for a full-time Clinical Research Coordinator to join our Research team. Overall, the Clinical Research Coordinator is t...
Schedule subjects for appointments, procedures, or inpatient stays as required by study protocols.Perform specific protocol procedures such as interviewing subjects, taking vital signs, and performing electrocardiograms.Assess eligibility of potential subjects through methods such as screening inter...
We are seeking a highly motivated Senior Research Associate to join our Oncology Research team. ...
Work closely with visiting scientists, research collaborators and other laboratory team members on research projects as assigned by the Principal Investigator. Work closely with visiting scientists, research collaborators and other laboratory team members on research projects as assigned by the Prin...
We are seeking a skilled and dynamic Research and Data Assistant with strong administrative skills and experience in public health data management to join EpIC. The Assistant will also support EpIC by managing datasets, performing basic data analysis, and assisting with research and analysis project...
Knowledge of and interest in project management technology, such as document management systems, project extranets, databases, collaboration portals, SharePoint, Smartsheet, HighQ, or Microsoft Project. Experience with project management technology, such as document management systems, project extra...
Position Information Posting Number: 20245063V Position Title: Undergraduate Research Assistant - Kraut Lab Posting Type Student Hours/week: 35 Hours per week/ 10 weeks Eligibility: Work study preferred but open to all students Semester 2024 Summer Location Mendel Science Center Detailed Work Schedu...
The Practice Facilitator (PF) will:.Build a trusting relationship with clinic leadership and champions to serve as a resource for each clinic to improve the provision, uptake, and sustained delivery for PrEP to WWID;.Provide logistical support to clinics, including helping the champion troubleshoot ...
We handle all types of commercial projects, both single-trade and multi-trade projects for the multi-site industry such as remodels, painting, fencing, etc. Maintain tracking systems for all pending, active and completed projects including but not limited to documentation uploads, status and schedul...
Research coordinator work includes study design, protocol development, submission to review boards, subject recruitment and enrollment, study visits and regulatory compliance in one or more studies. Involvement in trials will range from consulting to serving as the primary coordinator for a study ha...
Consent patients and coordinate visits, lab blood draws and tissue acquisition.Collect, process, and ship biospecimens.Abstract data from electronic medical records.Accurately and efficiently enter data into REDCap.Assist in the creation, organization, and maintenance of spreadsheets and databases.A...