On-Site Clinical Research Coordinator — Protocols & Data
$38.23 - $42.21 per hourUniversity of California, San Francisco
A prominent research university in San Francisco is hiring a Clinical Research Coordinator to manage and coordinate clinical research protocols. This full-time position requires attention to detail, strong interpersonal skills, and the ability to multitask in a fast-paced environment. The ideal candidate will have a high school diploma with relevant experience and strong communication abilities. The salary for this role ranges from $38.23 to $42.21 per hour and offers a fully on-site work style. #J-18808-Ljbffr University of California, San Francisco
$43.78 per hour
...Clinical Research Coordinator Heluna Health invites applications for one full-time... ...a temporary, in-person/on site, full time, grant funded, benefitted... ...of a subset of study protocols, under the guidance of the... ...tracking systems; maintain data collection forms, logs, and...DataWebsiteHourly payFull timeTemporary workWork at officeAfternoon shift- Job Description The Clinical Research Coordinator supports several projects in the Division... ...several research protocols, including protocols for two... ...compensation; medical record data abstraction; administering... ...staff at UCSF and at primary site to ensure procedures are...DataWebsiteWork experience placement
- Responsibilities Research Operations Management... ...executives and coordinate documentation and... ...scenarios within the clinic trials and... ...ability to execute protocol safely and properly... ...industry using collected data to understand... ...Flexible 2 Days On-Site Employee Referral...DataWebsiteFull timeContract workLocal areaFlexible hoursShift work
$34.32 - $55.19 per hour
...organizational skills to serve as a Clinical Research Coordinator. Within the Multiple... ...and coordinating research protocols as directed by the Clinical... ...(PI). They may coordinate data collection and operations for... ...SF) Work Style: Fully On‑Site Shift: Days (8 Hours, 8:30...DataWebsiteHourly payWork experience placementWorldwideShift work$37.12 - $40.98 per hour
Clinical Research Coordinator (Phlebotomy) Job Summary Division of HIV, Infectious Diseases and... ...Coordinators with implementing study protocols, study coordination, data/specimen collection, data... .... Schedule Work Style: Fully On‑Site Shift: Days Shift Length: 8 Hours...DataWebsiteHourly payWork experience placementWork at officeLocal areaWork from homeWorldwideMonday to FridayShift workAfternoon shiftEarly shift$30.8 - $33.32 per hour
...the supervision of a Clinical Research Supervisor or Principal... ...to the support and coordination of clinical studies,... ...more single or multi‑site, active or follow‑up... ...trials; help prepare protocols for study initiation;... ...design flow sheets, data forms and source documents...DataWebsiteHourly payFull timeWork experience placementWorldwideMonday to FridayShift work$28.48 - $45.8 per hour
Assistant Clinical Research Coordinator MED-CORE-PULM Full Time 84335BR Job Summary... ...(a test of lung function), data abstraction from electronic... ...for writing/editing study protocols, and submitting IRB... ...the Parnassus and Mt. Zion sites), the Pulmonary and Critical...DataWebsiteHourly payFull timeWork experience placementWorldwideShift work- ...the supervision of the Clinical Research Supervisor, Clinical Research Coordinators (CRC) support the management... ...of study initiation of protocols are developed after... ...protocol files, data collection and subject... ...activities with non-UCSF sites. Problems in either of...DataWebsitePart timeWork at office
- ...the supervision of a Clinical Research Supervisor or Principal... ...Assistant Clinical Research Coordinator (CRC) supports and... ...more single or multi‑site clinical trials and... ...follow‑ups according to protocol. Provides calendars and... ...and/or studies. Data Management Abstracts...DataWebsite
- Overview The Assistant Clinical Research Coordinator will perform independently or with... ..., and coordinate research protocols, as directed by the... ...Investigator (PI); may coordinate the data collection and operations... ...of specimens to central sites. Ensure integrity and security...DataWebsiteWork experience placementLocal areaWorldwideFlexible hours
$60k - $140k
...Clinical Research Coordinators Wanted Clinical Research Coordinators wanted at Medpace! Become... ...closeout visits at research sites in compliance with the approved protocol Communication with the... ...verification against case report form data, including informing the site...DataWebsiteFull timeContract workTemporary workWork at officeLocal areaImmediate startRemote workWork from homeHome officeFlexible hours- ...Nurix Therapeutics is a clinical stage biopharmaceutical... ...monitors and clinical sites throughout the life cycle... ...timeline, and study protocol Works closely with investigative... ...Collaborate with Data Management to ensure... ...guidelines, and coordinate delivery of data updates...DataWebsiteContract work
$34.32 - $55.19 per hour
A leading research institution is seeking a Clinical Research Coordinator to manage and coordinate clinical research studies in... ...regulatory compliance, and assisting in data management and reporting.... ...medical records. This is a fully on-site position in San Francisco, CA,...DataWebsiteHourly pay$160k - $185k
...Senior Clinical Trial Manager San Francisco, CA or Remote or... ...through close-out (including site activation, enrollment,... ...Monitor study metrics, including data quality, protocol deviations, and site... ...Support cross-functional coordination across Clinical, Regulatory...DataWebsiteRemote workFlexible hours- ...worldwide. The Clinical Trial Manager (CTM... ...at the trial and site level. The CTM will... ...Heartflow Clinical Research staff and... ...clinical research coordinators, principal investigators... ...the development of protocols, informed consent... ...including core labs and data management...DataWebsiteWork experience placementWork at officeLocal areaWorldwideRelocationShift work
- Overview The Clinical Trial Manager (CTM) will provide... ...oversight of clinical sites, etc. Obtain and review... ...GCP, regulations, the protocol, and company SOPs/Policies... ...house review of clinical data listings for... ...functional team May lead and coordinate protocol deviation review...DataWebsiteContract workFor contractorsWork at officeRemote work
- ...Carolina and Boston) clinical-stage biotechnology company... ...Phase 2b with topline data expected in 2027.... ...trial includes clinical sites in China, which is... ...visits, and training coordination Track and reconcile China... ...site metrics to ensure protocol compliance and data quality...DataWebsitePart timeLocal areaRemote workRelocationFlexible hours
- ...Under the supervision of a Clinical Research Supervisor or Principal... ...to the support and coordination of clinical studies and... ...of one or more single site clinical studies; help prepare protocols for study initiation; help... ...design flow sheets, data forms and source documents...DataWebsiteRelocation
- UCSF Health is looking for a Clinical Research Coordinator to join the Pediatric Oncology/Hematology research team in San Francisco. In this role, you will independently manage and coordinate research protocols while ensuring compliance with UCSF policies. The ideal candidate...
- ...Senior Clinical Trial Manager South San Francisco... ...budget, and with high data quality and compliance... ...study execution from protocol development through CSR... ...assessments and support site selection strategy... ...and cross-functional coordination skills ~ Comfortable...DataWebsiteContract workInterim role
- ...Responsibilities: Research and Early... ...The gRED Global Clinical Trial Leader (CTL)... ...limited or no clinical data, requiring the implementation... ...to the Protocol Execution Team (PET... ...on study plans and coordinate effective investigator... ...to country and site selection, assist...DataWebsiteLocal areaFlexible hours
$120k - $140k
...Reporting to the Director, Clinical Operations, the Clinical Trial... ...milestones and deliverables from protocol creation to study completion.... ...monitoring oversight and routine data cleaning Contribute to the... ...review of study plans, ICFs, site manuals, patient materials, CRF...DataWebsitePart timeWork at officeWork from homeFlexible hours$143k - $175k
...Clinical Trial Manager, CKD South San Francisco... ...trials; from protocol development to achievement... ...investigative sites. Ensure... ...investigative sites. Coordinate the development of... ...4 years clinical research experience,... ...to industry market data to ensure we pay competitive...DataWebsiteInterim roleWork at office- ..., Inc. (Nura Bio) is a clinical-stage biopharmaceutical... ...neurological diseases. Nura Bio's research and early development... ...adherence to clinical protocols, SOPs, ICH-GCP, and... ...e.g., slow enrollment, data quality issues) and... ...travel as required for site visits, audits, and meetings...DataWebsiteFlexible hours
- ...Clinical Research Coordinator The Clinical Research Coordinator, under the oversight of the Clinical Trial... .... These sessions will be conducted on-site in South San Francisco and virtually.... ...device accountability, and completing data entry into the Electronic Data Capture...DataWebsiteWork experience placement
- ...Position Title: Global Clinical Trial Leader (CTL)... ...or no clinical data, requiring the... ...The Organization’s Research and Early Development... ...cross-functional Protocol Execution Teams (... ...on study plans and coordinate effective... ...Contribute to country and site selection, assist...DataWebsiteLocal areaRemote workMonday to FridayFlexible hours
- ...University of California - San Francisco is seeking a Clinical Research Coordinator to manage investigator-sponsored research studies. This role involves overseeing study protocols, recruiting and enrolling subjects, managing data collection, and ensuring compliance with...Data
$130k - $142.5k
...Clinical Trial Manager, Oncology, Asia Eikon... ...quality study data, on time and on budget... ...functions (Site Engagement & Monitoring... ...adherence to study protocols, regulatory... ...investigators, study coordinators, and study site personnel... ...to oncology research Demonstrated experience...DataWebsiteSummer holidayWork at office3 days per week$37.12 - $40.98 per hour
A leading research university in California seeks a Clinical Research Coordinator to support HIV research projects at Zuckerberg San... ...candidate will facilitate study protocols and coordinate participant... ...the role requires presence on-site Monday through Friday. #J-1880...WebsiteHourly payMonday to Friday- ...University of California at San Francisco to serve as a Clinical Research Coordinator (CRC) in the DeRisi and Wilson Laboratories. This... ...series to execute, manage, and coordinate research protocols; coordinate the data collection and operations of several concurrent clinical...DataFlexible hours
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