The Clinical Research Budget Coordinator I develops clinical trial budgets for industry, National Institutes of Health (NIH), and investigator-initiated clinical research. Evaluates research protocols to assess resource needs for research procedures, clinical research staff time, investigator time, ...
The Clinical Research Finance Coordinator I develops clinical trial budgets for industry, National Institutes of Health (NIH), and investigator-initiated clinical research. Evaluates research protocols to assess resource needs for research procedures, clinical research staff time, investigator time,...
The Clinical Research Finance Coordinator I develops clinical trial budgets for industry, National Institutes of Health (NIH), and investigator-initiated clinical research. Evaluates research protocols to assess resource needs for research procedures, clinical research staff time, investigator time,...
The Clinical Research Budget Coordinator I develops clinical trial budgets for industry, National Institutes of Health (NIH), and investigator-initiated clinical research. Evaluates research protocols to assess resource needs for research procedures, clinical research staff time, investigator time, ...
We are seeking a detail-oriented and experienced Unblinded Coordinator to join our clinical research team. The Unblinded Coordinator will play a critical role in maintaining the integrity of our clinical trials by managing all unblinded activities. Collaboration: Work closely with the study team, in...
As a Clinical Research Coordinator I, you will work independently providing study coordination including screening of research participants for protocol eligibility, presenting non-medical trial concepts and details, and participating in the informed consent process. Clinical Research Coordinator I ...
The Clinical Research Finance CoordinatorI develops clinical trial budgets for industry, National Institutesof Health (NIH), and investigator-initiated clinical research. Evaluates research protocols to assess resource needs for researchprocedures, clinical research staff time, investigator time, an...
The Assistant Clinical Research Coordinator assists the Clinical Research Coordinator and/or Senior Clinical Research Coordinator in contributing to the overall operational management of clinical research/trial/study activities. Ability to adapt to changing job demands and priorities; work flexible ...
The ADRC is an interdisciplinary group of researchers including faculty investigators, research coordinators, health professionals, and trainees who are committed to research on memory problems and aging. The ADRC Research Coordinator will work with USC investigators and research staff to coordinate...
This position is suitable for an individual interested in gaining hands-on research conducting basic and clinical research on child development and enjoys working in a team of clinicians, researchers, and (under)graduate students. Attention to detail in scheduling families for research, coordinating...
As our Clinical Research Coordinator (CRC), you will support multiple clinical research studies ensuring adherence to federal/local/institutional regulatory requirements, good clinical practice, data quality, protocol compliance, protection of human subjects, and overall quality assurance and qualit...
The Research Administrative Coordinator works under the direction of the Research Director; Research Manager; and the Research Operations Associate of the assigned research area. Research Admin Coordinator - Cheng Lab, Heart Institute. The Smidt Heart Institute reflects Cedars-Sinai's steadfast dedi...
The Greater Los Angeles Veterans Research and Education Foundation (GLAVREF) seeks an enthusiastic Clinical Research Coordinator (CRC) to join our dynamic clinical trials team. EXPERIENCED Clinical Research Coordinator - Onsite. Experienced in IRB processes, federal research regulations and a basic ...
The Clinical Research Coordinator I works independently providing study coordination, screening of potential patients for protocol eligibility, presenting non-medical trial concepts and details, and participating in the informed consent process. Responsible for compiling and reporting on each study ...
Prepare and process all Institutional Review Board (IRB)through the IRB and other regulatory groups as apropriate including initial submissions, amendments, continuing reviews, adverse events and serious adverse events.Coordinate, organize and maintain all documentation required by sponsor or CRO (c...
The Clinical Research Coordinator II works independently providing study coordination including screening of patients for protocol eligibility, presenting non-medical trial concepts and details, and participating in the informed consent process. Responsible for compiling and reporting on each study ...
As an Associate Clinical Research Coordinator (ACRC), you'll play a pivotal role in ensuring the integrity of research studies. Associate Clinical Research Coordinator-Duarte. With a focus on maintaining updated patient data in the clinical research management system, your contribution will be integ...
National Institute of Clinical Research, a research organization serving the pharmaceutical and biotech industries, is searching for a Clinical Research Coordinator with 2 or more years of experience. REQUIREMENTS: A minimum of 2 years of clinical research experience is preferred. In-depth knowledge...
Coordinate and conduct clinical studies, includes; subject recruitment, informed consent, chart maintenance and data entry.Coordinate IRB submissions and renewals in accordance with FDA and IRB guidelines.Assure compliance with the protocol and regulatory requirements includes: collecting, recording...
We’re seeking a self-motivated, independent professional with: * Five or more years of experience as a study coordinator for clinical research * Data management experience with clinical research protocols * Knowledge of health services or clinical research methodology and principles * IRB experience...
The Research Nurse Coordinator III is responsible for all activities associated with clinical study coordination, subject enrollment, data management/integrity, regulatory compliance, project/study evaluation and interfacing with participants and family members. Coordinates the clinical logistics of...
Facilitating and supporting studies and research as needed. ...
As a Clinical Research Coordinator I, you will work independently providing study coordination including screening of research participants for protocol eligibility, presenting non-medical trial concepts and details, and participating in the informed consent process. Work alongside physician-scienti...
The Assistant Clinical Research Coordinator assists the Clinical Research Coordinator and/or Senior Clinical Research Coordinator in contributing to the overall operational management of clinical research/trial/study activities. The Assistant Clinical Research Coordinator recognizes and performs nec...
Assisting with writing research results and grant reports. Leading annual holiday suicide myth research project. Recruiting undergraduate student coders, training them to work on content analysis and other quantitative and qualitative research projects, and assessing inter-coder reliability using Kr...