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
- ...Description Job Title: Assistant Clinical Research Coordinator Location Address: Palo... ...prefer oncology and treatment trials, as well as EPIC knowledge... ...collection of clinical data and/or the coordination of... ...and documents, including consent forms and master subject logs...DataFull timePart timeRemote workShift workNight shift
- ...is dedicated to researching the effect of... ...interventions through clinical research. We... ...Research Coordinator to manage study... ..., high-quality data collection, and... ...questionnaires; Ensure consent documentation... ...procedures; Assist in training research... ...completion of trial activities....DataNight shift
- ...Assistant Clinical Research Coordinator The Precision Neurotherapeutics Lab in the Department... ...recruiting, and gathering consent from study participants... ...other psychophysiological data for clinical research... ...subjects upon completion of trial activities. Assist with post...DataFull time
$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$160k - $170k
...their skills.The Sr. Clinical Trial Manager (Sr CTM) is responsible... .... Provides any assistance with findings from... ...level issues/trends in data and EDC metrics reporting. Assist in coordinating study specific training... ...information/informed consents and completes associated...DataFull timeTemporary workWork experience placementWork at officeRemote workFlexible hours- ...Assistant Clinical Research Coordinator A leading university is seeking an Assistant Clinical Research Coordinator... ...with participant recruitment, data collection, regulatory documentation... ...with recruitment, screening, informed consent, follow-up communications, and...Data
- ...Perioperative, and Pain Medicine seeks a Clinical Research Coordinator 2 (CRC2) for a fixed‑term 2‑year... ...will coordinate complex industry‑sponsored trials in critical care and OR settings, recruit participants, and manage data across the study lifecycle. Responsibilities...DataFixed term contract
- Stanford Radiology is seeking a Clinical Research Coordinator 2 (CRC2) to support complex imaging studies in a dynamic research environment... ..., sponsors, and partners to coordinate multi-site trials, regulatory activities, data management, and study finances. You will recruit...Data
- ...of Medicine invites applications for a Clinical Research Coordinator 2 (CRC2) on a fixed-term 2-year... ...spans multiple complex industry-sponsored trials in ICU and OR settings, with long-term... ...You will lead recruitment, manage study data, collaborate with nurses, pharmacy staff...DataFixed term contract
- Stanford University in Stanford, CA seeks a Clinical Research Coordinator 2 (Fixed-term 2 years) to manage multiple complex industry-sponsored trials in ICU/OR, including sepsis, ARDS, and AKI. The CRC2 will recruit, collect data, and ensure protocol adherence across...DataFixed term contractNight shift
- ...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...DataFixed term contract
- 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
$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 roleLocal areaWorldwide$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 roleLocal areaWorldwide$146.54k - $189.64k
...ensuring that Gilead clinical trials are conducted in compliance... ...high-quality clinical data that supports global... ..., may lead contract research organization (CRO) and... ...protocols, and informed consents, oversees/authors... ...meetings).Leads or otherwise assists in the preparation of...DataFull timeContract workFor contractorsFor subcontractorInterim roleLocal areaFlexible hours$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 roleLocal areaWorldwide- ...DescriptionWe are seeking a Clinical Trials Manager (CTM) to... ...study management by coordinating with the internal... ...aspects of clinical study.Assists Clinical Program... ...protocols, informed consents, case report forms, monitoring... ...review of data listings and preparation...DataFull timeContract workFor contractorsInterim roleWork at officeLocal area
$35 - $70 per hour
...Title: Clinical Research Coordinator Pay Rate Range: $35.00 - $70.... ...oncology and other clinical trials within affiliated... ...-out. Screen, consent, and enroll participants... ...timely and accurate data entry. Maintain patient... ...efforts and assist in developing patient...DataFull timeContract workWork at officeMonday to FridayAfternoon shift- Stanford University Department of Dermatology seeks an Assistant Clinical Research Coordinator to support data collection and coordination of clinical studies, including dermatology trials. The role operates under supervision of the principal investigator and research manager...Data
- 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 in Palo Alto is seeking a Clinic Clinical Research Coordinator Associate (CRCA) to coordinate oversight and implementation of neuromuscular... ...eligibility, coordinating specimen collection, managing data and study documents, and ensuring IRB renewals. #J-18808...Data
- ...Pediatrics is seeking a highly organized Clinical Research Coordinator Associate to advance a multi-site comparative effectiveness ADHD trial in young children at our Stanford site... ...include participant contact, consent, data management, regulatory submissions, monitor...Data
- Stanford University’s Department of Dermatology is seeking an Assistant Clinical Research Coordinator (ACRC) to perform administrative support duties related to the collection of clinical data and the coordination of clinical studies. The ACRC will support federal and...Data
- ...Veterans Institute for Research (PAVIR is looking... ...for a full-time Clinical Research Coordinator I . The Research... ...screen, recruit, consent, and enroll... ...assessments. Assist with specimen collection... .... Enter study data into electronic... ..., clinical trial and research data...DataFull timeTemporary workWork at office
- 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
- Job Title: Clinical Research Coordinator Type: Full-Time We are hiring a Clinical... ...interventional, IND-enabled trials, the scope of this role will... ...logs. Administer informed consent, including confirming... ...resolve queries, and maintain data quality to audit-ready standards...DataFull timeRemote work
- Clinical Trial Manager, Clinical Operations Job Type... ...standards for data quality, compliance... ...to and coordinate the review of clinical... ...protocols, informed consent forms, case report... ...to Clinical Research Associates. Monitor... ...monitoring reports and assist with the...DataFull time
$156.6k - $184.3k
...receptor antagonists. With advanced clinical trials in patients with hypercortisolism,... ...vendors to ensure high quality of data. Providing Clinical Research Associates with project‑specific training... ...study documents such as informed consent form templates, site management,...DataFull timeWork at office3 days per week- ...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
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