Introduction to Clinical Research: Clinical Trial Phases and Design. Course Developer - Clinical Research, Regulatory Affairs, and Biotechnology - UC Berkeley Extension. UC Berkeley Extension, the professional and continuing education division at the University of California, Berkeley, seeks dynamic...
The Clinical Research Coordinator will provide research support for the Pediatric Emergency Care Applied Research Network (PECARN) clinical research program. The Clinical Research Coordinator will work with faculty, fellows and residents to organize and participate in all operational aspects of ongo...
Introduction to Clinical Research: Clinical Trial Phases and Design. UC Berkeley Extension, the professional and continuing education division at the University of California, Berkeley, seeks dynamic part-time online course developers with a commitment to undergraduate, professional, and continuing ...
Experience performing clinical research duties in a clinical research environment. Experience performing clinical research duties in a clinical research environment. Directly communicate with physicians and clinical staff to review study data and provide routine updates to the clinical research team...
The UCSF Fresno Clinical Research Coordinator will perform independently or with general direction at the fully operational journey level of the series to execute, manage, and coordinate research protocols, as directed by the Clinical Research Manager and Principal Investigators (PIs); may coordinat...
Experience performing clinical research duties in a clinical research environment. Experience performing clinical research duties in a clinical research environment. Clinical Research Coordinator Assistant - TP132384. TES is currently hiring for a Clinical Research Coordinator Assistant. ...
Some conduct bench research in wet lab settings; others have dry lab (computer based) research programs or specialize in clinical research. Many of our faculty conduct research activities and manage large research staffs, including students, fellows, post docs, and staff research associates. Clinica...
Reporting directly to the Disease Team Project Manager, the Clinical Research Coordinator I is responsible for coordinating and managing clinical trials including providing all aspects of protocol management, including screening for patient eligibility, data collection and analysis, ensuring protoco...
Assist Principal Investigators in the conduct of research by providing nursing expertise in the education and monitoring of patients involved in clinical trials and other research studies, in the collection and analysis of patient data, and in the preparation of research documents for the sponsoring...
Reporting to the Gynecologic Oncology Clinical Research Manager, the Clinical Research Coordinator 2- will be conversant in the goals, mission and priorities of the Institute, and utilize this knowledge. Society of Clinical Research Associates or Association of Clinical Research Professionals certif...
As a Clinical Research Coordinator III, you will work independently providing study coordination including screening of potential research participants for protocol eligibility, presenting non-medical trial concepts and details, and participating in the informed consent process. This position is res...
The Clinical Trial Research Coordinator I (CTRC-I) is a novice level position which, under the clinical direction of the Principal Investigator (PI), assists in the operational and administrative research support of the Kaiser Permanente Northern California (KPNC) PI and KPNC Clinical Trials Operati...
As a Clinical Research Associate focused on medical devices, you will play a crucial role in the planning, execution, and monitoring of clinical trials. You will ensure that studies are conducted in accordance with regulatory requirements, Good Clinical Practice (GCP), and company policies. Assist i...
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. Maintains research practices usi...
The Child Life Clinical Lead provides assistance for the Child Life Manager with both administrative and clinical supervision tasks. Oversees and ensures that direct reports complete clinical competencies in a timely manner and provides support for those individuals when applying for clinical advanc...
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 ...
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...
Researches new and/or improves test development methodologies. Researches new and/or improves test development methodologies by: performing experimental testing procedures; validating effectiveness/feasibility for implementation; costing of procedure(s); preparing and submitting recommendation(s) fo...
The Clinical Research Coordinator will be responsible for multiple administrative tasks related to the organization of multiple internal and external clinical Client sponsored trials including IRB submissions, along with upkeep of clinical documentation as necessary. Assist the field Clinical Develo...
The Lead Clinical Research Associate manages the design, execution, and monitoring of internal and external clinical studies, coordinates the development of operating procedures, coordinates in the development of standard procedures in executing experiments, evaluation, and documentation of results,...
The Lead Clinical Research Associate manages the design, execution, and monitoring of internal and external clinical studies, coordinates the development of operating procedures, coordinates in the development of standard procedures in executing experiments, evaluation, and documentation of results,...
Introduction to Clinical Research: Clinical Trial Phases and Design. UC Berkeley Extension, the professional and continuing education division at the University of California, Berkeley, seeks dynamic part-time online course developers with a commitment to undergraduate, professional, and continuing ...
Worldwide Clinical Trials (Worldwide), a leading global contract research organization (CRO), works in partnership with biotechnology and pharmaceutical companies to create customized solutions that advance new medications – from discovery to reality. ...
The Clinical Research Coordinator will be responsible for multiple administrative tasks related to the organization of multiple internal and external clinical Client sponsored trials including IRB submissions, along with upkeep of clinical documentation as necessary. Assist the field Clinical Develo...
The clinical laboratory scientist performs routine and complex laboratory procedures in a prompt, accurate and reliable manner according to established procedures and quality control guidelines. Bachelor's Degree in Medical Technology or related field of Life Science with Clinical Laboratory Science...