In this role, you'll be instrumental in conducting examinations, blood draws, and specimen collection on research subjects. ...
Participate in clinical research teams to ensure the most effective and efficient conduct of clinical research studies by providing training, protocol interpretation, document collection and review and overall clinical trial support. Bachelors degree with 4+ year experience as a Clinical Trials Asso...
A company is looking for a Principal Clinical Research Scientist with CRO Experience Required for a remote position. ...
The UCLA Center for LGBTQ+ Advocacy, Research, and Health (C-LARAH) is part of the Fielding School of Public Health, within the Department of Epidemiology. The mission of C-LARAH is to maintain an interdisciplinary, research-driven, evidence-based platform used to carry out public policy initiatives...
The Clinical Research Coordinator II is crucial to the companies clinical research, managing multiple complex trials across various areas and phases. An exciting Clinical Site Network are looking to bring on board a Clinical Research Coordinator to either of their sites based out of. Minimum of 3+ y...
Contribute to all clinical research activities to ensure successful management of clinical studies under the direct supervision of Clinical Affairs manager with dotted lines to clinical study manager. The Senior Clinical Research Associate will report to Manager, Clinical Affairs, and will play a ke...
Research, Good Clinical Practice (GCP), Federal Regulations pertaining to research, and applicable guidance’s and regulations. USC Norris Comprehensive Cancer Center - CISO is seeking a Clinical Research Program (Disease Team) Manager. Supervises – Disease Team Study and Research Coordinators who pr...
The Clinical Research Coordinator II works independently providing study coordination including 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 e...
Serve as lead coordinator on a portfolio of Chemo/Onc research studies. ...
With minimal supervision, the Clinical Research Coordinator II (CRC-II) is responsible for providing coordinator support to multiple human subjects’ (clinical) research projects and is expected to perform all core Clinical Research Coordinator (CRC) responsibilities. Association of Clinical Research...
We seek a detail-oriented Clinical Research Data Coordinator to utilize their initiative and organizational skills to keep our research moving at top performance. At least 2 years of Clinical Research Coordinating Experience under a PI at a Research Site/Facility. Clinical Research Data Coordinator....
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, ...
Promote good clinical practice in the conduct of clinical investigations, included possessing an in-depth knowledge of the federal regulations and guidance documents for the conduct of clinical studies and human subject protection. Coordinate and conduct clinical studies, includes; subject recruitme...
Under the direction of Research Institute Management, the Clinical Research Nurse Coordinator II is responsible for providing coordinator assistance for sponsored clinical studies within the Center for Clinical Research in accordance with Institutional policy, Good Clinical Practice and ICH guidelin...
Clinical research nurses are tasked with communicating clinical protocols to patients and also conveying patient data to research coordinators. ALOIS Healthcare is seeking a travel nurse RN Research / Clinical Research for a travel nursing job in Los Angeles, California. Posted job title: RN:Clinica...
Overall, the successful candidate will have experience working in a clinical trials research environment, and will have familiarity with data management, have excellent organizational skills, work well as a member of a small research team, be able to work independently, and have the ability to inter...
Acquires and utilizes knowledge of clinical trial design to develop specific study concept sheets and protocols. Anticipates moderately complex obstacles within a clinical study and with guidance implements solutions. Excellent verbal and written communication skills and interpersonal skills are req...
The Clinical Research Associate I works directly with a Clinical Research Coordinator, Research Program Administrator, or Research Nurse to coordinate and/or implement the study. Works with a Clinical Research Coordinator, Research Program Administrator or Research Nurse to coordinate/implement stud...
Overview Purpose Statement/Position Summary: The Clinical Research Coordinator I assists principal investigators or other study team members with research studies and assists with subject recruitment, data collection, scheduling of study-related activities and follow-up with enrolled subjects. Certi...
The Clinical Research Associate (CRA) is responsible for establishing and maintaining the Study Master File, tracks critical trial information, and supports Regional Clinical Research Associates under the guidance of a Clinical Manager or Clinical Director. Obtains site documents from Regional Clini...
Provide clinical research support to investigators to prepare for and execute assigned research studies, including:. Review study protocols, Case Report Forms (CRFs), other study-specific documents, and electronic data capture systems used to record clinical research data;. Collect and submit regula...
Association of Clinical Research Professionals Certified Professional (ACRP-CP), Certified Clinical Research Professional (CCRP) or Certified Clinical Research Coordinator (CCRC). Preferred: Clinical research experience in a hospital setting and/or pediatric clinical research experience. Required: M...
Excellentknowledge of Clinical Research methods andprocedures. Scor other diploma from a Clinical Researchprogram. Avalid Clinical Researchlicense. Yourexpertise and opinions shall be valuable to us which shall help usin ourresearch. ...
Job Description Grow your career at Cedars-Sinai! Join our team and use your skills with an organization known nationally for excellence in research! This position functions as a Clinical Research Finance Coordinator (CRFC) responsible for coordinating and executing the financial billing of clinical...
As a Clinical Research Associate at Parexel, you will be joining a team with a wide variety of experiences and knowledge. Your hard work may be rewarded through a bonus incentive program, the opportunity to work within multiple therapeutic areas and an opportunity to advance your career in clinical ...