Search jobs > Santa Clara, CA > Clinical research coordinator
A company is looking for a Clinical Research Finance Coordinator II (Pre-Award) to manage financial aspects of clinical research studies during the pre-award phase.
Key ResponsibilitiesDevelop and negotiate complex clinical trial budgets for various research studiesMonitor study accounts, reconcile payments, and manage invoicing for sponsorsPerform Medicare coverage analysis and collaborate with the Institutional Review Board (IRB) for budget approvalsRequired QualificationsHigh School Diploma or equivalent required;
Bachelor's Degree in Accounting, Finance, or related field preferredMinimum of 3 years of experience in billing, accounting, finance, budgeting, or financial analysisAt least 1 year of experience in clinical research
Clinical Research Coordinator
Nursing, Biology, Public Health)Minimum of 1 year of experience in clinical researchKnowledge of Good Clinical Practice (GCP), FDA regulations, and IRB processesExperience with electronic medical records (EMR) systems is a plusCertification in clinical research (e. A company is looking for a Clinica...
Clinical Research Coordinator 2
Parker Center for Allergy and Asthma Research at Stanford University is seeking a Clinical Research Coordinator 2 (CRC2) to manage life-changing clinical trials under the direction of project researchers, investigators, or managers. Primary responsibilities as a CRC2 will include the oversight and c...
Cancer Clinical Research Coordinator Associate - Sarcoma Oncology
Reporting to Clinical Research Manager for Sarcoma 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 r...
Clinical Research Coordinator
Serve as primary contact with research participants, sponsors, and regulatory agencies for research projects within our Lung Transplantation team. Serve as primary contact with research participants, sponsors, and regulatory agencies for research projects within our Lung Transplantation team. Collec...
Assistant Cancer Clinical Research Coordinator - Network (South Bay) at Stanford University
Reporting to the SCI-CTO Network Clinical Research Manager, the Assistant Cancer Clinical Research Coordinator will be conversant in the goals, mission and priorities of the Institute as well as the Network research sites, and utilize this knowledge to conduct industry sponsored trials, cooperative ...
Assistant Clinical Research Coordinator
The Department of Radiation Oncology is hiring Assistant Clinical Research Coordinators to support the clinical research of several faculty physicians. The Assistant Clinical Research Coordinator will perform administrative support duties related to the collection of clinical data and/or the coordin...
Clinical Research Coordinator (CRC)
Clinical Research Coordinator (CRC). Stirling Q&R is seeking a dedicated and detail-oriented Clinical Research Coordinator on behalf of our confidential client. Join our client in a dynamic environment where you will have the opportunity to contribute to groundbreaking research while advancing y...
Clinical Research Coordinator I - Kerlan Jobe Institute
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 ...
Clinical Research Coordinator I, Salvy Lab (Onsite)
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 ...
Clinical Research Coordinator II (Hybrid), Breast
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...