Clinical Research Coordinator: Trials & Compliance Pro
Stanford University
Stanford University is seeking a Clinical Research Coordinator Associate to manage multiple protocols at Stanford Hospital and Clinics. You will work with a team of investigators to prepare IRB submissions, aid amendments and renewals, recruit and consent participants, and maintain data files per GCP and HIPAA guidelines. The role involves data collection, blood sample handling, drug accountability, and reporting adverse events to investigators and sponsors. Evening/weekend hours may be required. #J-18808-Ljbffr Stanford University
- ...Otolaryngology - Head and Neck Surgery division seeks a clinical research coordinator to oversee recruitment, data management, and study operations... ...in OHNS. You will supervise staff, ensure regulatory compliance (HIPAA, FDA), manage budgets, and collaborate with investigators...Suggested
- Stanford University is seeking a Clinical Research Coordinator Associate to oversee the management and implementation of multiple research protocols... ...Hospital and Clinics. You will ensure regulatory compliance, assist with IRB submissions, consent processes, data collection...Suggested
- .... Stanford University is seeking a Clinical Trial Regulatory lab manager (Clinical Trials... ...the administration and regulatory compliance of clinical research within SINC, and representing the... ..., participants, and study coordinators. This position is a 1-year fixed term...SuggestedFixed term contractLocal area
$30 - $31 per hour
...Job Title: Clinical Research CoordinatorJob Description This role provides... ...of research data and the coordination of clinical studies. You work... ..., efficiently, and in compliance with established protocols... ...participants upon completion of trial activities. + Assist with...SuggestedContract workTemporary workWork at officeNight shift3 days per week$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- Stanford University is seeking a Clinical Trial Regulatory Lab Manager for the Stanford Innovative Neurotherapeutics Center (SINC) to oversee regulatory compliance of clinical research within SINC and act as the university's liaison with external regulatory agencies, both...
- ...Medicine invites applications for a Clinical Research Coordinator 2 (CRC2) on a fixed-term 2-year appointment... ...multiple complex industry-sponsored trials in ICU and OR settings, with long-... ...investigators, ensure regulatory compliance, and support budget tracking and regulatory...Fixed term contract
- Stanford University seeks a Clinical Research Coordinator 2 (CRC2) to coordinate a dynamic portfolio of complex clinical trials in critical care and operating room settings. You will recruit, enroll, and follow participants, collaborate with PIs, nurses, and pharmacy staff...
- Stanford University in Palo Alto is seeking an experienced Clinical Research Coordinator 2 to support study start-up activities across interventional and observational trials. You will coordinate start-up, manage budgets, provide metrics, and ensure regulatory approvals...
$160k - $170k
...grow and develop their skills.The Sr. Clinical Trial Manager (Sr CTM) is responsible for effective... ....Review monitoring reports for compliance to study protocols, regulations and ICH... ...and EDC metrics reporting. Assist in coordinating study specific training or re-training...Full timeTemporary workWork experience placementWork at officeRemote workFlexible hours$175k - $189k
...Sr. Clinical Trial ManagerSynthekine is a Menlo Park, CA based biotechnology... ...study team activities and coordinate operational deliverables... ...resolution, quality performance, and compliance with study requirements.... ...that govern clinical research, including but not limited to...Work at officeLocal area$146k - $161k
...Clinical Trial Manager/Senior Clinical Trial Manager Waltham, Massachusetts, United States... .... Role Overview: Will ensure trial compliance, regulatory alignment, and operational... ...alignment, risk management and coordination across all participating functions....Work at officeRemote work3 days per week- Ascendis Pharma is seeking a Sr. Clinical Trial Manager to lead global and regional trials, based in Palo Alto or remote. The role reports to the Director, Clinical Operations and requires 7+ years in managing Phase 1-3 trials, with strong ICH-GCP knowledge and cross-functional...Remote job
- ...Division of Gastroenterology and Hepatology seeks an Assistant Clinical Research Coordinator Associate to support 4-6 clinical studies on-site under... ...data, and handling administrative tasks while ensuring compliance with regulatory requirements. The position offers...
$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- Ascendis Pharma is seeking a Sr. Clinical Trial Manager to lead global and regional clinical trials from Palo Alto or remote. You will... ...relationships, monitoring, data quality, TMF maintenance, vendor coordination, and regulatory submissions, contributing to patient-focused...Remote jobWorldwide
- Palo Alto Veterans Institute for Research (PAVIR) is seeking a Clinical Research Coordinator II to support day-to-day operations of one or more clinical studies. The role works closely with the Principal Investigator, sponsors, regulatory bodies, and participants to ensure...Full time
- ...Assistant Clinical Research Coordinator 1503779 ~ Hourly pay: $34/hr ~ Worksite: Leading university (Palo Alto, CA 94304 - Hybrid) ~ W2 Employment... ...documentation, and study operations while ensuring compliance with research protocols and regulatory requirements....Hourly payShift work3 days per week
- Stanford Cancer Institute is seeking a Clinical Research Coordinator 2 to support the Blood and Marrow Transplant/Cell Therapy programs. You will... ...recruitment, data management, budgeting, and regulatory compliance while mentoring staff and coordinating with investigators...
$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$30 - $31 per hour
...Description Job Description Job Title: Clinical Research Coordinator Job Description This role provides... ...accurately, efficiently, and in compliance with established protocols and regulatory... ...for participants upon completion of trial activities. Assist with post-study...Contract workTemporary workWork at officeNight shift3 days per week- 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...
- Stanford University is seeking a Clinical Research Coordinator for the Otolaryngology - Head and Neck Surgery division. This two-year fixed-term... ...recruitment, data collection, budgeting, and regulatory compliance in a fast-paced research environment. The successful candidate...Fixed term contract
- ...location.Job Summary: We are seeking a Clinical Trials Manager (CTM) to support the Oncology... ...study execution and study management by coordinating with the internal teams and external... ...documents to ensure that CROs /vendors are in compliance with protocols, regulatory...Full timeContract workFor contractorsInterim roleLocal area
$106k - $132k
Revolution Medicines is a late-stage clinical oncology company developing... ...Phase I-III clinical trials in an industry setting and a... ...be responsible for Contract Research Organization (CRO) oversight... ...on time, within budget and in compliance with Standard Operating Procedures...Full timeContract workFor contractorsInterim roleLocal area- ...worldwide execution of all Phase I - IV clinical trials across all Gilead therapeutic areas.... ...are met.With guidance, may lead contract research organization (CRO) and vendor selection... ...documents to ensure that CROs /vendors are in compliance with protocols, regulatory requirements...Full timeContract workFor contractorsFor subcontractorInterim roleLocal areaWorldwideFlexible hours
$33 - $37 per hour
...Job Title: Clinical Research Data CoordinatorJob Description This role supports oncology clinical trials by entering, validating, and managing complex clinical research data... ...capture systems. The Clinical Research Data Coordinator maintains and enhances databases,...Contract workTemporary work$40 per hour
...of their needs, we are looking for a Clinical Research Coordinator 2 Job Description: Job Title... ...participants in long-term clinical trials. Oversee data management for research... ...laboratory procedures, to ensure compliance with applicable regulations; provide...Contract workWork at officeNight shift$51.72 per hour
...of their needs, we are looking for a Clinical Research Coordinator Job Description: Job Title:... ...Associate The Clinical Trials Office in the company, in company Medicine... .../case report forms. *Ensure compliance with research protocols, and review and...Contract workWork at office- ...Stanford University’s Department of Neurosurgery is seeking a Clinical Research Coordinator to perform duties related to the coordination of... ...clinical reality. This position includes managing device trials for neuromodulation, conducting longitudinal natural history...Full timeAfternoon shift
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