The Clinical Research Associate I will work directly with a Clinical Research Coordinator, Research Program Administrator, or Research Nurse to coordinate and/or implement the study. This role evaluates and abstracts research data and ensures compliance with protocol and research objectives. The inc...
Working knowledge of clinical or laboratory research, clinical trial recruitment, eligibility, protocol adherence, quality data submission, and adverse event reporting. A longstanding program of research at the Memory and Aging Center is entitled Frontotemporal Dementia: Genes, Images, and Emotions:...
The core research team is comprised of a full time Research Compliance Analyst with a MPH and 2 years of clinical trials management experience who will be responsible for supervision and implementation of all active research protocols, two undergraduate level part time administrative support staff a...
The candidate will have leadership skills and training experience to provide operational leadership to a group of Clinical Research Staff, including a Clinical Research Supervisor, Senior Clinical Research Coordinator(s, and Clinical Research Coordinators (total program size of ~ 6-9 staff), while m...
We are seeking a detail-oriented and experienced Unblinded Coordinator to join our clinical research team. Minimum of 2 years of experience in clinical research, with specific experience in drug accountability or unblinded roles preferred. The Unblinded Coordinator will play a critical role in maint...
The Clinical Research Coordinator II serves as the lead coordinator on an assigned portfolio of research studies, functioning independently to establish and coordinate logistics and processes for the conduct of research for the department. Plans and coordinates strategies for increasing research par...
The ClinicalResearch Coordinator I works independently providing studycoordination, screening of potential patients for protocoleligibility, presenting non-medical trial concepts and details, andparticipating in the informed consent process. Responsible for compiling andreporting on each study inclu...
Reporting to Clinical Research Manager for Radiation Oncology, the Clinical Research Coordinator Associate will be conversant in the goals, mission and priorities of the Institute, and utilize this knowledge to manage data, enroll and follow patients on trial and assist with regulatory and financial...
Minimum one (1) year of training and/or experience in research methodology/research study design, hypothesis testing; OR Minimum one (1) year of experience in clinical trials protocols involving research methodology/research study design, and hypothesis testing; OR Minimum one (1) year experience in...
As a consortium cancer center, it is a collaborative partnership between the UCSD: encompassing 28 departments, 6 schools (School of Medicine, Skaggs School of Pharmacy and Pharmaceutical Sciences, School of Public Health, Jacobs School of Engineering, School of Biological Sciences & the School of P...
Responsible for the site visits, monitoring, communication and deliverables for the assigned study sites Serves as a member of the clinical study team and is the liaison between Clinical Operations and Study Site personnel for the specific clinical projects. If you have at least 5 full years of regi...
The CRC II may assist with the training and/or mentoring of CRC I or other CRC II staff on the basics of clinical research, Good Clinical Practice (GCP), Good Documentation Practices (GDP), Standard Operating Procedures (SOPs) and other related aspects of the clinical study. Responsible for the over...
Responsibilities include working with the research team(s), clinical staff, and Stanford Health Care departments to support conduct of safe and compliant clinical research. Society of Clinical Research Associates or Association of Clinical Research Professionals certification is preferred. We seek a...
The Clinical Research Associate II works directly with a Clinical Research Coordinator, Research Program Administrator, or Research Nurse, or Principal Investigator to coordinate and/or implement the study and may serve as the point of contact for the external sponsors. Works with a Clinical Researc...
Serve as lead coordinator on a portfolio of Chemo/Onc research studies. ...
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...
The Clinical Research Associate is the clinical sites’ direct point of contact and accountable for managing site quality and delivery from site identification through close-out. The Clinical Research Associate will oversee the conduct of the trial at designated sites, ensuring the rights and well-be...
Clinical research nurses are tasked with communicating clinical protocols to patients and also conveying patient data to research coordinators. Nurses are often responsible for providing both qualitative and quantitative data to research coordinators, which calls for keen powers of analysis. ...
Exciting opportunity for a detail-oriented individual! Join us as a DPS Clinical Research Assistant I in which you will manage an assigned set of multiple research protocols to assure efficiency and regulatory compliance of the protocol. Join the forefront of groundbreaking research at theBeckman Re...
The Clinical Research Informatician is a bridge between clinicians/researchers and data. They blend their knowledge of clinical workflow, terminology, and practices with an understanding of health information technology to advance clinical and translational research towards improved patient care. Cl...
The Clinical ResearchAssociate I works directly with a Clinical Research Coordinator,Research Program Administrator, or Research Nurse to coordinateand/or implement the study. Evaluates and abstracts research dataand ensures compliance with protocol and research objectives. Responsible for completin...
This professional will report to Clinical Science and External Research (CSER) Leaders in the management of assigned clinical projects for the Cardiovascular Group to support the development of the evidence generation and dissemination strategy of assigned products, manage clinical studies, execute ...
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...
The Clinical Research DataSpecialist I manages the data for assigned research studies. Maintains researchpractices using Good Clinical Practice (GCP) guidelines. Clinical Research Data Specialist I - PER_DIEM -HeartInstitute. Cedars-Sinai is home to some of the most advanced biomedicalresearch and t...
Job Description Are you looking to contribute to groundbreaking research? We look forward to having you join our team to collaborate on groundbreaking research! The Clinical Research Specialist provides clinical research expertise by participating in the design and implementation of research project...