To perform the duties of Principal Investigator on non-First in Human clinical trials according to International Conference on Harmonisation (ICH) Good Clinical Practice and to the highest standard to ensure that the welfare of the trial participants and the quality and credibility of study data is ...
Provide leadership in the management and operation of clinical research protocols to ensure research participant recruitment and accrual, protocol compliance, research participant safety and data quality. CCRP - Cert Clin Research Prof (Preferred) or CCRC - Cert Clin Research Coordinator (Preferred)...
SOP(Standard Operating Procedure).SDV: Source Data Verification).IRB (Institutional Review Board)....
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...
We are seeking motivated individuals to make an academic contribution to the Mitochondrial Myopathy Clinical Research program, which focuses on validation of objective outcome measures in Mitochondrial Myopathy for natural history studies and clinical trials in its clinical research effort, and deve...
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 ...
Under minimal supervision, the coordinator will facilitate all clinical research activities within the scope of the clinical research protocols. This is a full-time or part-time Clinical Research Coordinator position offered through Clinical Futures at Children's Hospital and Safe Place: The Center ...
Clinical Research Assistant A will perform research and administrative tasks for research projects and clinical trials within the Penn Department of Medicine’s Clinical Trials Unit. Prescreen, recruit, consent (minimal risk) and screen patients according to protocol; Schedule patient visits and any ...
The CRC will be responsible for the coordination of complex oncology clinical research protocols, including accurate data collection and overseeing the quality of the clinical trial data and records, scheduling and conducting study initiation and monitoring visits, and participating in ongoing study...
Clinical Research Coordinator in Media, PA (19063). Bachelor's Degree; 1+ Years of Clinical Research Coordinating experience. ...
Clinical Research Assistant A will perform research and administrative tasks for research projects and clinical trials within the Penn Infectious Diseases Clinical Trials Unit (ID CTU). Clinical Research Assistant A:. Involvement in trials will range from several weeks to serving as the primary rese...
Coordinator B: Participate in and coordinate clinical trials within the Penn Division of Infectious Disease Clinical Trials Unit, consisting of projects in HIV, COVID19, and other Infectious Diseases. The person will support Infectious Disease Investigators in clinical research ranging from observat...
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...
Job Title: Clinical Research Nurse. We are seeking a Clinical Research Nurse with extensive experience in oncology and strong experience as a Registered Nurse. The ideal candidate will have over 5 years of experience in clinical research and will be comfortable interacting with physicians. The resea...
Correspond with the IRB and manage protocols including drafting initial submission documentation, modifications, continuing reviews, and audits, 2) Coordinate research activities with collaborating institutions, including collecting, uploading, processing data from multiple clinical sites, and estab...
Provides leadership in the management and operation of clinical research protocols to ensure research participant recruitment and accrual, protocol compliance, research participant safety and data quality. Coordinates and facilitates the conduct of clinical research protocols which may be supported ...
Over this period, the CRI has conducted clinical research trials and other research projects that have transformed the practice of radiology, informed the development of clinical practice standards, led to new device approvals, and changed healthcare policy. Consistent with the ACR’s mission to adva...
Provide leadership in the management and operation of clinical research protocols to ensure research participant recruitment and accrual, protocol compliance, research participant safety and data quality. Coordinate and facilitate the conduct of clinical research protocols which may be supported by ...
Oncology Clinical Research Nurse. Work closely alongside PI and clinical research coordinators. Minimum of 3 years of Clinical Research Nurse experience. If no Clinical Research Nurse experience, must have a minimum of 1 year of Oncology experience AND 3 years of nursing experience in a clinic setti...
Provide supervision and support for other clinical research coordinators and or/ monitors who are assigned to specific protocols and who will help with the overall clinical research of the program. Applied knowledge of Good Clinical Practice (GCP) guidelines including protection of human research su...
While the PI and Site Manager are responsible for the overall design, conduct, and management of the clinical trial, you support, facilitate, and coordinate the daily clinical trial activities and play a critical role in the conduct of the study including supporting patients throughout the clinical ...
The Clinical Research Coordinator, in collaboration with the Clinical Investigators at the Lewis Katz School of Medicine, will be responsible for the planning, implementation, and execution of Clinical Trials in the assigned department. Clinical Research Coordinator (Recruitment Only)-(16001534). Re...
Clinical Research Coordinators (CRC) perform protocol specific duties relevant to the clinical trial. Identify and enroll qualified participants for ongoing and new clinical trials, through collaboration with PIs, use of study portals, and other tools. ...
We’re proud to foster an inclusive environment driving innovation and excellence, and we welcome you to join us on our mission to shape the future of clinical development as a Clinical Research Associate II. ICON plc is a world-leading healthcare intelligence and clinical research organization. Cond...
General experience and knowledge of database applications and theory, clinical research software systems, medical research methods and operations, medical terminology and computer report generation software; and financial, HR, EHR, and Grants Systems Design and Implementation (Preferred). Advance th...