Clinical Research Coordinator — Trials & Compliance Lead
Stanfordlivetickets
Stanford University is seeking a Clinical Research Coordinator Associate to oversee the management and implementation of multiple research protocols at Stanford Hospital and Clinics. You will ensure regulatory compliance, assist with IRB submissions, consent processes, data collection, and CRF preparation, working with Principal Investigators. Responsibilities include recruitment, subject scheduling and follow-up, adverse event reporting, drug accountability, and maintaining study supplies, #J-18808-Ljbffr Stanfordlivetickets
- 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,...SuggestedWeekend workAfternoon shift
$45 - $50 per hour
...Clinical Research Coordinator Hourly pay: $45-$50/hr Worksite: Leading university (Palo Alto, CA 94304 - Hybrid) W2 Employment... ...recruitment through regulatory compliance, data management, and sponsor... ...oncology treatment trials. ~ Experience supporting Phase...SuggestedHourly payWork at office- The Department of Medicine's Clinical Research Hub at Stanford University seeks a Clinical Research Coordinator Associate to coordinate nephrology, hospital medicine and other trials in both inpatient and outpatient settings; onsite with direct patient contact. You will...Suggested
- ...University’s Department of Medicine, Clinical Research Hub seeks a Clinical Research Coordinator Associate to support... ...of infectious disease and other trials. This onsite role involves direct... ...collecting data and specimens, ensuring compliance with IRB and #J-18808-Ljbffr...Suggested
$156.6k - $184.3k
...antagonists. With advanced clinical trials in patients with hypercortisolism... ...(when applicable) to ensure compliance with protocol and the... ...goals. May serve as a Study Lead to the multifunctional team... ...of data. Providing Clinical Research Associates with project‑specific...SuggestedFull timeWork at office3 days per week- 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...
$44 - $50 per hour
Clinical Research Coordinator (Position ID 1497945) - Hourly pay: $44-$50/hr - Location: Leading university, Stanford, CA 94305 - Hybrid (3-4 days onsite). Job Overview... ...aspects of oncology clinical trials while ensuring regulatory compliance, participant safety, and high-...Hourly payWork at officeShift work- Stanford University is seeking an Assistant Clinical Research Coordinator to support NIH-funded trials evaluating AI-based behavioral interventions in the emergency department. The role involves recruiting, enrolling, and following up with participants, collecting data...
- 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
$175k - $189k
...has raised $313M from leading biotech investors. We... ...collaborative Senior Clinical Trial Manager (Sr. CTM) to... ...team activities and coordinate operational deliverables... ...performance, and compliance with study requirements... ...that govern clinical research, including but not limited...Work at officeLocal area$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. This role entails serving... ...for research participants and ensuring compliance with protocols while managing critical research...Hourly pay- TEKBERRY is hiring a Clinical Research Coordinator in Palo Alto, CA. The role focuses on coordinating clinical studies, managing recruitment, data collection, and regulatory compliance. The position is contract-based with potential extension and hybrid onsite work. Qualifications...Contract work
- 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...
- 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
$84.86k - $97.02k
A leading educational institution in California is seeking a Clinical Research Coordinator Associate for clinical research projects in pediatric oncology. This full-time, entry... ...studies, managing data, and ensuring compliance with research protocols. Ideal candidates...Full timeWork at office- 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 Dermatology is seeking a Clinical Research Coordinator II to lead and manage complex clinical studies, coordinating cross‑functional... ...oversight of key study activities, regulatory compliance, and data integrity in busy clinical environments. The...
$120k - $150k
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.... ...goals are met.With guidance, may lead contract research organization (CRO) and vendor... ...to ensure that CROs /vendors are in compliance with protocols, regulatory requirements...Full timeContract workFor contractorsFor subcontractorInterim roleLocal areaWorldwideFlexible hours
$157.59k - $203.94k
...and help create possible, together.Job DescriptionClinical Operations leads the global execution of Phase I-IV clinical trials across therapeutic areas, ensuring studies are conducted in compliance with SOPs, company policies, and regulatory requirements while delivering...Full timeFor contractorsLocal area- ...-sponsored and cooperative group cancer trials from start-up to close-out, with a hybrid work arrangement. Reporting to the Clinical Research Manager of Study Start-Up, the role requires... ...communication skills and the ability to lead multidisciplinary teams. A Bachelor's...
- Eudia in Palo Alto is seeking a Trial Program Manager to own the technical and operational execution of enterprise trials from kickoff... .... You will serve as the single point of accountability, coordinating Sales, Product, and the customer during the evaluation window....
- ...Clinical Trial Manager The Clinical Trial Manager (CTM) will manage... ...functional execution to meet them Coordinate and oversee CROs and vendors... ...data collection, protocol compliance, and completion of key study... ...engineering, clinical research, or related field; advanced...
$86.25k - $100.16k
...Neurosurgery is seeking a Clinical Research Coordinator II (CRCII) to conduct clinical... ...may include drug/ device trials, longitudinal natural history... ..., as assigned. Lead team meetings and prepare/approve... ...laboratory procedures, to ensure compliance with applicable regulations...Full timeContract workWork at officeLocal areaAfternoon shift$40 per hour
...needs, we are looking for a Clinical Research Coordinator 2 Job Description:... ...participants in long-term clinical trials. Oversee data... ...accountabilities, as assigned. Lead team meetings and prepare/approve... ...procedures, to ensure compliance with applicable regulations...Contract workWork at officeNight shift$51.72 per hour
...needs, we are looking for a Clinical Research Coordinator Job Description:... ...Associate The Clinical Trials Office in the company, in... ...guidelines. company strives to lead the biomedical revolution... ...forms. *Ensure compliance with research protocols, and...Contract workWork at office$48 - $50 per hour
...Jobs # Job Description Clinical Research Coordinator Contract: Palo Alto, California,... ...equivalent. Oncology treatment trial experience, preferably Phase I.... ...submissions/renewals and maintain regulatory compliance with FDA and HIPAA requirements....Hourly payContract workTemporary workRelocation$37 - $45 per hour
...Clinical Research Coordinator-Oncology Onsite 5 Days Qualifications + MUST HAVE 2 years of experience as... ...CRC), preferably with complex clinical trials + MUST HAVE hands-on experience... ...eligibility + Demonstrated ability to ensure compliance with research protocols and...Contract workTemporary work$146.54k - $189.64k
...patients for generations to come.Clinical Operations is responsible for... ...of all Phase I - IV clinical trials across all Gilead therapeutic... ...study teamsPlans and coordinates all operational activities required... ...on trackOrganizes and leads Biomarker and Bioanalytical operational...Full timeFor contractorsInterim roleLocal areaWorldwide- Eudia Counsel, LLC is seeking a Trial Execution Specialist to own the technical and operational delivery of enterprise trials from kickoff to decision. You will serve as the connective tissue between Sales, Product, and customers, ensuring the trial runs on time and to...
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