Assistant Clinical Research Coordinator: Data, Consent & Trials
Stanford University
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 documents, consent forms, and scheduling calls with participants. The role includes screening and consenting participants, administering questionnaires, collecting data, performing basic measurements under protocol, and assisting #J-18808-Ljbffr Stanford University
- ...to the collection of clinical data and/or the coordination of clinical studies.... ..., including consent forms and master subject... ...correspondence. Assist with the screening,... ...source documents for research studies as directed.... ...upon completion of trial activities. Assist with...DataNight shift
- ...Assistant Clinical Research Coordinator 2Hourly pay: $30/hrWorksite: Leading university (Palo... ...participant coordination, data collection, and study... ...recruiting, and obtaining consent from study participants, including... ...letters to subjects upon trial completion, and assist...DataShift workDay shift3 days per week
$28.59 - $32.9 per hour
...University is seeking an Assistant Clinical Research Coordinator to perform administrative... ...the collection of clinical data and/or the coordination of... ...and documents, including consent forms and master subject logs... ...upon completion of trial activities. Assist with post...DataHourly pay$29.44 - $33.26 per hour
...Stanford University is seeking an Assistant Clinical Research Coordinator Associate (aCRC) to support... ...-sponsored drug or device trials. The aCRC will assist with study coordination, data collection, and... ...regulatory documents; maintain consent forms, master subject logs,...DataHourly payFull time- ...Assistant Clinical Research CoordinatorThe Precision Neurotherapeutics... ...Assistant Clinical Research Coordinator. The primary focus... ..., and gathering consent from study participants... ...psychophysiological data for clinical research... ...subjects upon completion of trial activities. Assist...DataFull time
$84.86k - $97.02k
Clinical Research Coordinator 2 (Fixed-term 2 years) Stanford, CA, United... ...complex clinical trials in various stages of... ...responsible for managing data related to study outcomes... ...hiring, preparing or assisting with the preparation... ...obtaining informed consent in a hospital setting...DataFull timeContract workTemporary workPart timeFixed term contractWork at officeFlexible hoursNight shift- ...Stanford Prevention Research Center (SPRC) is a consortium... ...and experienced Assistant Clinical Research Coordinator (ACRC) with strong... ...obtaining informed consent from participants;... ...reviewing participant data to ensure... ...upon completion of trial activities. Assist with...DataFixed term contractNight shift
- ...contributions in basic research, a new commitment to clinical and outcomes research,... ...diseases. The Assistant Clinical Research Coordinator Associate (aCRC) will... ...sponsored drug or device trials. Responsibilities include... ...study coordination, data collection, and administrative...Data
- ...Our client is currently seeking a Assistant Clinical Research Coordinator Job Title: Assistant Clinical... ...support related to clinical data collection and clinical study coordination... ...Maintain regulatory documents, consent forms, subject logs, and study correspondence...Data3 days per week
- Stanford University is seeking a Clinic Research Coordinator Associate in the Neuromuscular Division of... ...sponsors, ensuring regulatory compliance, data accuracy, and efficient study... ...while supporting investigator-initiated trials in neuromuscular disorders. #J-18808-...Data
- Actalent is seeking a Clinical Research Coordinator in Palo Alto, CA to support interventional drug trials under a principal investigator. The role involves data collection, regulatory documentation, and direct interaction with participants. You will help ensure protocol...Data
- The Stanford Prevention Research Center (SPRC) at Stanford University... ...of Medicine is seeking an Assistant Clinical Research Coordinator (ACRC) to help recruit... ...handling informed consent, guiding participants to radiology, and ensuring data completeness. Fluency in target...Data
- Stanford University is seeking a Clinical Research Coordinator Associate to oversee the management and implementation of multiple... .... You will ensure regulatory compliance, assist with IRB submissions, consent processes, data collection, and CRF preparation, working with...Data
- ...Role: Senior Clinical Trial Manager overseeing global oncology Phase 2/3 trials, including NSCLC and colorectal cancer, with responsibilities... ...site selection, enrollment, monitoring, risk management, and data quality, ensuring regulatory compliance and quality standards...Data
$40 per hour
...Clinical Research Coordinator 4 1520994 ~ Hourly pay: $40/hr ~ Worksite... ...eligibility and gather consent according to protocol, assist in developing... ...patient and laboratory data, manage research project... ...coordinating oncology treatment trials. ~ Experience using...DataHourly payWork experience placementWork at officeShift workDay shift3 days per week$120k - $150k
...Medicines is a late-stage clinical oncology company... ...I-III clinical trials in an industry... ...responsible for Contract Research Organization (CRO)... ...labs, Electronic Data Capture (EDC)... ...manuals, informed consent forms and clinical... ...reconciliation process. Assistance with the...DataFull timeContract workFor contractorsInterim roleLocal area$120k - $150k
...for an experienced Clinical Operations... ...Phase I-III clinical trials in an industry setting... ...responsible for Contract Research Organization (CRO)... ...labs, Electronic Data Capture (EDC)... ...manuals, informed consent forms and clinical... ...process. Assistance with the preparation...DataFull timeContract workFor contractorsInterim roleWorldwide- Stanford University invites applications for a clinical research professional to support the Sean N. Parker Center for Allergy and Asthma Research. The role focuses on recruitment, data management, budgeting, regulatory compliance, and collaboration with investigators...Data
- Stanford University’s Gastroenterology and Hepatology division seeks an Assistant Clinical Research Coordinator Associate to support 4-6 studies on-site under supervision. You will assist with coordination, data collection, questionnaires, and regulatory tasks, contributing to...Data
- Stanford University is seeking a Clinical Research Coordinator II (CRCII) to conduct clinical research and independently manage complex studies in... ...site work at Stanford. Responsibilities include recruitment, data management, budgeting, and IRB/IND submissions as...DataWeekend workAfternoon shift
- Stanford University in Palo Alto invites applications for an Assistant Clinical Research Coordinator Associate (aCRC) to support 4-6 clinical studies under... ...supervisor. You will assist with study coordination, data collection, biospecimen handling, and regulatory tasks to...Data
- ...Clinical Research Coordinator The Clinical Trials Office in the company, in company Medicine seeks... ...and to document related data per protocols and SCI-CTO... ...eligibility of and gather consent from study participants according to protocol. Assist in developing recruitment...DataWork at office
- ...looking for an experienced Clinical Research Coordinator to support and manage... ...research, treatment trials, onsite clinical study... ...and obtain informed consent according to study protocols. Assist with participant recruitment... ...and laboratory data. Maintain research databases...DataFull timeContract workWork experience placementWork at office3 days per week
- Job Title: Clinical Research Coordinator Location: Palo Alto, CA 94304- Hybrid... ...requirements: Clinical research assistant and data entry experience, have... ...and documents, including consent forms and master subject... ...upon completion of trial activities. Assist with post...Data3 days per week
$30 - $31 per hour
Job Title: Clinical Research Coordinator (Thoracic)Job Description This... ...patient safety, accurate data collection, and... ...facilitate the informed consent process, ensuring... ...procedures and requirements. Assist in developing and... ...of treatment trials. Demonstrated experience...DataContract workTemporary workWork at officeRemote work3 days per week$37 - $45 per hour
Job Title: Clinical Research Coordinator 2 Job Description This role leads... ...smaller clinical trials. The position... ...and requires strong data management, regulatory... ...subject recruitment, consent, enrollment, and follow... ...Transportation benefits Employee Assistance Program Time Off/...DataContract workTemporary workWork at office$30 - $37 per hour
Job Title: Clinical Research Coordinator Job Description This role provides... ...interventional drug trials. You will work under... ..., detailed data collection and management... ...related requirements. Assist with screening, recruiting... ...obtaining informed consent from study participants...DataContract workTemporary workWork at office- ...Department of Dermatology is seeking an Assistant Clinical Research Coordinator (ACRC) to perform administrative... ...related to the collection of clinical data and the coordination of clinical... ...investigative work in support of clinical trials, clinical research, or biomedical...Data
- ...Cardiothoracic Surgery, Division of Thoracic Surgery seeks a Clinical Research Coordinator Associate to coordinate moderately complex studies. The... ...principal investigators and residents in grant preparation, data management, and manuscript preparation. Ideal candidates...DataWork at office
$146.54k - $189.64k
...region)s of assigned clinical studies, multiple... ...may lead contract research organization (CRO)... ..., and informed consents, oversees/authors... ...support clinical trials.May be required to... ...Leads or otherwise assists in the preparation... ...including resolving any data discrepancies....DataFull timeContract workFor contractorsFor subcontractorInterim roleLocal area
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