Clinical Research Coordinator: Trials & IRB Compliance
Stanford University
The Clinical Research Coordinator Associate at Stanford University works with Stanford Hospital and Clinics to manage multiple research protocols, ensuring regulatory compliance and efficient study conduct. You will recruit and screen participants, obtain informed consent, coordinate data collection, and monitor subject safety, reporting adverse events as required. The role reports to Principal Investigators and involves IRB submissions, budget monitoring, and collaboration with sponsors and #J-18808-Ljbffr Stanford University
Vacancy posted 4 hours ago
Similar jobs that could be interesting for youBased on the Clinical Research Coordinator: Trials & IRB Compliance in Palo Alto, CA vacancy
- ...Summary Collects data for clinical trials research, following general directions... ...regulatory bodies (e.g., IRB) for pre‑implementation review... ..., under guidance, in compliance and consistency with all applicable... ...clinical sites, and data coordinating centers as applicable; and...SuggestedTemporary workFor contractorsFor subcontractorLocal area
$35 - $45 per hour
Leading university in the Stanford, CA area is seeking a Clinical Research Coordinator to support coordination and execution of clinical studies... ...participants, sponsors, and regulatory agencies, ensuring protocol compliance and accurate documentation. The role involves...Suggested$44 - $50 per hour
...Clinical Research Coordinator (Position ID 1497945) – Hourly pay: $44-$50/hr – Location: Leading university, Stanford, CA 94305... ...independently manage key aspects of oncology clinical trials while ensuring regulatory compliance, participant safety, and high-quality study...SuggestedHourly payWork at officeShift workAvispa Technology
Palo Alto, CA4 days ago$35 - $45 per hour
...Clinical Research Coordinator Hourly pay: $35-$45/hr Worksite: Leading university (Stanford, CA 94305 -... ...and regulatory agencies while ensuring compliance with research protocols, maintaining... ...supporting the successful conduct of clinical trials. Responsibilities Coordinate all...SuggestedHourly payWork at officeShift workResearch And Developement Industries Inc
Palo Alto, CA3 days ago$156.6k - $184.3k
...glucocorticoid receptor antagonists. With advanced clinical trials in patients with hypercortisolism,... ..., and CROs (when applicable) to ensure compliance with protocol and the overall clinical... ...quality of data. Providing Clinical Research Associates with project‑specific...SuggestedFull timeWork at office3 days per week- ...University’s School of Medicine seeks a Clinical Research Coordinator 2 (CRC2) for a fixed-term 2-year... ...portfolio of industry‑sponsored clinical trials in various life-cycle stages.... ...management, budgeting, and regulatory compliance; the role #J-18808-Ljbffr Stanford UniversityFixed term contract
$35 - $45 per hour
Assistant Clinical Research Coordinator 1500902 Hourly pay: $35-$45/hr Worksite: Leading university (Palo... ...research operations while ensuring compliance with institutional, sponsor, and... ...documentation by preparing and maintaining IRB submissions, protocol amendments,...Hourly payWork at officeFlexible hoursShift work$37 - $45 per hour
...Job Description Job Title: Clinical Research Coordinator – Oncology Job... ...complex oncology clinical trials from study start-up through... ...documentation, and ensure strict compliance with protocols and regulatory... ...Institutional Review Board (IRB) renewals are completed on...Contract workTemporary workShift work$34.56 - $40.3 per hour
...Neuromuscular Division of Neurology is seeking a Clinical Research Coordinator Associate (CRCA) to coordinate the... ...assuring efficiency and regulatory compliance. Responsibilities Serve as primary... ..., data management, FDA regulations, IRB requirements and the Stanford...Hourly payWork experience placementWork at office$86.25k - $100.16k
...Neurosurgery is seeking a Clinical Research Coordinator II (CRCII) to conduct clinical... ...may include drug/ device trials, longitudinal natural history... ...procedures, to ensure compliance with applicable regulations... ...Experience with local and single-IRB submissions. Experience...Full timeContract workWork at officeLocal areaAfternoon shiftWomen Veterans Interactive
Palo Alto, CA1 day ago$35 - $70 per hour
...Clinical Research Coordinator Pay Rate Range: $35.00 $70.00/hr (DOE, based on experience... ...and other clinical trials within affiliated research... ...safely, efficiently, and in compliance with federal, institutional... ...according to protocol and IRB requirements. Schedule and...Full timeContract workWork at officeMonday to FridayAfternoon shift$34.56 - $40.3 per hour
A leading medical institution is seeking a Cancer Clinical Research Coordinator Associate to oversee clinical studies in the Melanoma-Oncology area... ...primary contact for research participants and ensuring compliance with protocols while managing critical research data....Hourly pay$120k - $150k
Evommune, Inc. (NYSE: EVMN) is a clinical-stage biotechnology company... ...a highly motivated Clinical Trial Manager to support the... ...site performance, protocol compliance, data quality, and monitoring... ...Investigational Product release coordination and site activation...Work at officeRemote work2 days per week3 days per week- ...University is seeking a Cancer Clinical Research Coordinator Associate - GI Hybrid to support GI oncology trials within the Stanford Cancer... ...safety, regulatory compliance, and accurate data management... ...clinical research background, IRB familiarity, strong communication...
$86.25k - $100.16k
...Neurosurgery is seeking a Clinical Research Coordinator II (CRCII) to conduct clinical... ...may include drug/device trials, longitudinal natural history... ...procedures, to ensure compliance with applicable regulations... ...Experience with local and single‑IRB submissions. Experience...Full timeContract workWork at officeLocal areaAfternoon shift$84.86k - $97.02k
...leading educational institution in California is seeking a Clinical Research Coordinator Associate for clinical research projects in pediatric... ...involves coordinating studies, managing data, and ensuring compliance with research protocols. Ideal candidates will hold a bachelor...Full timeWork at office- Maxonic Inc. is seeking a Clinical Research Coordinator 2 to manage clinical research projects while ensuring compliance with regulatory standards. The ideal candidate will have a Bachelor's degree and two years of relevant experience in clinical research. Responsibilities...Work at office
- Women Veterans Interactive is looking for a Clinical Research Coordinator Associate in Palo Alto to join their Urology department. This role involves... ...clinical studies, managing patient data, and ensuring compliance with protocol. The ideal candidate should have a...Work at office
- Stanford University is seeking a Clinical Research Coordinator Associate to coordinate oversight and implementation of neuromuscular research protocols, ensuring efficiency and regulatory compliance across studies. The role involves serving as primary contact for participants...
- Stanford University is seeking an Assistant Clinical Research Coordinator to provide administrative support for clinical data collection and study coordination. You will work under the supervision of the principal investigator and study coordinators, handling regulatory...
$85k - $140k
...patients worldwide. The Clinical Trial Manager (CTM) is... ...the HeartFlow Clinical Research staff and collaborate... ...staff, clinical research coordinators, principal... ...documents (informed consents, IRB approvals, research agreements) to ensure compliance with study requirements...Remote jobWork experience placementWork at officeLocal areaWorldwideRelocationShift work$34.56 - $40.3 per hour
...program, and cutting-edge research, we work together to... ...opportunity for a Clinical Research Coordinator Associate to join... ...Pediatric Urology trials as well as multi-institutional... ...forms. Ensure compliance with research... ...regulations. Familiarity with IRB guidelines and...Hourly payWork experience placementWork at officeNight shiftWomen Veterans Interactive
Palo Alto, CA1 day ago$34.56 - $40.3 per hour
...University. We seek a Cancer Clinical Research Coordinator Associate to help us enact... .... The Cancer Clinical Trials Office (CCTO) is an integral... .../case report forms. Ensure compliance with research protocols, and... ...collection. Familiarity with IRB guidelines and regulations....Hourly payWork experience placementWork at officeAfternoon shiftStanford University School of Medicine
Palo Alto, CA2 days ago- Research And Developement Industries Inc in Palo Alto, CA is seeking an Assistant Clinical Research Coordinator to support the day-to-day coordination of clinical studies at a leading... ...research operations while ensuring compliance with institutional, sponsor, and regulatory...Part time
$34.56 - $40.3 per hour
...Clinical Research Coordinator Associate The Division of Child Neurology is seeking... ...efficiency and regulatory compliance. These studies will be conducted... ...work as part of a clinical trials research team and report to... ...study documents for IRB submission in compliance with...Hourly payFixed term contractWork experience placementWork at officeLocal areaAfternoon shift- Stanford University in Palo Alto, CA, seeks a Cancer Clinical Research Data Manager (Data Aide 3 - GI) to join the Clinical Trials Office. This hybrid role involves entering, verifying, and maintaining complex databases, developing data collection tools, and ensuring data...Work at office
$145k - $165k
...platform has demonstrated promising clinical data across multiple solid... .... Overview The Clinical Trial Manager has operations experience... ...overall quality, safety, and compliance throughout the duration of... ...or biotech‑related/clinical research, oncology or research experience...Work at officeLocal areaRemote workIovance Biotherapeutics, Inc.
San Carlos, CA1 day ago$51 per hour
...of their needs, we are looking for a Clinical Research Coordinator 2. Job Title: Clinical Research Coordinator... ...participants in long‑term clinical trials. Oversee data management for research... ...laboratory procedures, to ensure compliance with applicable regulations; provide...Contract workWork at officeMaxonic
Palo Alto, CA2 days ago- Evommune, Inc. is seeking a highly motivated Clinical Trial Manager to support the operational execution of company-sponsored clinical trials in Palo Alto, CA. The role involves managing timelines, risks, and performance in collaboration with CROs and clinical sites. The...
$120k - $150k
Evommune, Inc. in Palo Alto is seeking a Clinical Trial Manager to oversee the execution of clinical trials. The ideal candidate will have over 5 years of clinical operations experience, with strong capabilities in monitoring and managing trials in a fast-paced environment...Work at office2 days per week
Do you want to receive more vacancies?
Subscribe and receive similar vacancies to Clinical Research Coordinator: Trials & IRB Compliance. Be the first to apply!
Related searches
- clinical project manager Palo Alto, CA
- neuroscience clinical research coordinator Palo Alto, CA
- clinical trials manager Palo Alto, CA
- clinical research coordinator Palo Alto, CA
- associate director clinical research Palo Alto, CA
- clinical research lead Palo Alto, CA
- clinical research fellowship Palo Alto, CA
- clinical research remote Palo Alto, CA
- clinical research nurse Palo Alto, CA
- clinical trials Palo Alto, CA