Assistant Clinical Research Coordinator
Stanford University School of Medicine
Job Description The 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 pediatric clinical studies. This position requires in-person attendance on the main campus in Palo Alto. In this role, the ACRC will work under the supervision of the principal investigator and/or study coordinator/supervisor. Desired Qualifications A Bachelor’s degree with an educational background in medicine and/or scientific field (biological sciences, social sciences, etc.) Proven ability to work independently and take ownership of a project. Proven ability to work collaboratively and cooperatively in a team environment. Ability to work effectively in a fast-paced environment and balance multiple projects and timelines at one time. Strong oral and written communication skills. Detail-oriented with excellent organizational skills. Proficiency in using computers, software, and web-based applications in a previous administrative setting PHYSICAL REQUIREMENTS* Frequently stand, walk, twist, bend, stoop, squat and use fine light/fine grasping. Occasionally sit, reach above shoulders, perform desk based computer tasks, use a telephone and write by hand, lift, carry, push, and pull objects that weigh up to 40 pounds. Rarely kneel, crawl, climb ladders, grasp forcefully, sort and file paperwork or parts, rarely lift, carry, push, and pull objects that weigh 40 pounds or more. - Consistent with its obligations under the law, the University will provide reasonable accommodation to any employee with a disability who requires accommodation to perform the essential functions of his or her job. Working Conditions Position may at times require the employee to work with or be in areas where hazardous materials and/or exposure to chemicals, blood, body fluid or tissues and risk of exposure to contagious diseases and infections. May require extended or unusual work hours based on research requirements and business needs. Work Standards Interpersonal Skills: Demonstrates the ability to work well with Stanford colleagues and clients and with external organizations. Promote Culture of Safety: Demonstrates commitment to personal responsibility and value for safety; communicates safety concerns; uses and promotes safe behaviors based on training and lessons learned. Subject to and expected to comply with all applicable University policies and procedures, including but not limited to the personnel policies and other policies found in the University's Administrative Guide, Responsibilities Core Duties Schedule and/or call subjects for appointments; contact participants with reminders or other requirements. Prepare, distribute, and process questionnaires. Perform clerical duties in the preparation of regulatory documents. Maintain all forms and documents, including consent forms and master subject logs. File all appropriate correspondence. Assist with the screening, recruiting, and obtaining consent of study participants. Review medical records and/or perform telephone or in-person interviews to gather data, as needed. Administer standard study questionnaires and tests, score test measurements and questionnaires, and code data for computer entry. Perform quantitative review of forms, tests, and other measurements for completeness and accuracy. Extract data from source documents for research studies as directed. Collect data and complete case report forms. Perform basic measurements and tests on patients according to protocol, such as obtaining vital signs and performing phlebotomy and EKG, after appropriate training/certification. Collect study specimens according to protocol. Prepare, process, and ship specimens/samples accurately under well-defined requirements. Order and maintain equipment and supplies. Process study compensation payments and thank you letters to subjects upon completion of trial activities. Assist with post-study activities, as needed. Minimum Education And Experience Two-year college degree and one year of relevant experience or an equivalent combination of experience, education, and training. Knowledge, Skills And Abilities General knowledge of medical terminology. Certificates And Licenses Required Working toward certification(s) to perform basic patient measurements and tests, such as phlebotomy and EKG. Must possess and maintain a valid California non-commercial Class C Driver's License, if applicable. Drivers License Requirements Must possess and maintain a valid California non-commercial Class C Driver's License. Ability to drive day or night. When conducting university business, must comply with the California Vehicle Code and Stanford University driving requirements. #J-18808-Ljbffr
- ...stanford.edu ) in the Department of Psychiatry and Behavioral Sciences at Stanford University is seeking a full-time Assistant Clinical Research Coordinator (ACRC). The primary focus will be to assist with multiple NIH-funded projects to develop more personalized TMS...SuggestedFull time
$29.44 - $33.26 per hour
...The Division of Gastroenterology and Hepatology at Stanford University is seeking an Assistant Clinical Research Coordinator Associate (aCRC) to support 4–6 clinical research studies on-site under the supervision of the principal investigator or study supervisor. The position...SuggestedHourly payFull time- ...Description Job Title: Assistant Clinical Research Coordinator Location Address: Palo Alto, CA 94306 Duration of project : 06 Months( Start and end date - 05-Oct-2026 - 05-Mar-2027) Remote/onsite/hybrid: Hybrid and onsite 4 days per week during training Full...SuggestedFull timePart timeRemote workShift workNight shift
- ...and innovative center dedicated to excellence in research, medical education, and clinical care. Supported by more than 90 faculty members... ...disease. We are currently seeking an Assistant Clinical Research Coordinator (ACRC) who is passionate about clinical research...Suggested
- ...Job Description 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. This position is...SuggestedWork at office
- Stanford University’s Department of Dermatology seeks an Assistant Clinical Research Coordinator (ACRC) to support data collection and coordination of clinical studies. This hybrid role requires at least three days in the office weekly at the Redwood City Campus, reporting...Work at office
- ...Job Description Job Description Description: Temporary Assistant Clinical Research Coordinator Responsibilities: Assist with the preparation and submission of Institutional Review Board (IRB) protocols, amendments, continuing reviews, and related regulatory...Temporary workRemote workFlexible hoursShift work
- Stanford University is seeking a Clinical Research Coordinator 2 to conduct clinical research and work independently on progressively more complex... ...as assigned, potentially including hiring, preparing or assisting with the preparation of performance evaluations, and...Contract workWork at officeNight shift
- The Department of Medicine (DoM) Clinical Research Hub (CRH) at Stanford University is seeking a Clinical Research Coordinator 2 in Study Start Up Group to perform duties related... ...and forecasts to CRM and collaborators; assisting with development of effective budgets and...Contract workWork at officeLocal areaWorldwideNight shift
$86.25k - $100.16k
...Clinical Research Coordinator 2 The Department of Neurology at Stanford University is seeking a Clinical Research Coordinator 2 to conduct clinical... ...as assigned, potentially including hiring, preparing or assisting with the preparation of performance evaluations, and...Hourly payContract workWork at office- ...Stanford University’s Department of Neurosurgery is seeking a Clinical Research Coordinator to perform duties related to the coordination of... ...neuromodulation, conducting longitudinal natural history studies, and assisting with various PI-initiated projects involving adult...Full timeAfternoon shift
$51.72 per hour
...client. In support of their needs, we are looking for a Clinical Research Coordinator Job Description: Job Title: Clinical Research Coordinator... ...consent from study participants according to protocol. Assist in developing recruitment strategies. *Coordinate...Contract workWork at office$45 - $50 per hour
...Clinical Research Coordinator Hourly pay: $45-$50/hr Worksite: Leading university (Palo Alto, CA 94304 - Hybrid) W2 Employment, Group Medical, Dental, Vision, Retirement Savings Program, PSL 40 hours/week, 6 Month Assignment, Possible extension/conversion...Hourly payWork at office$72k - $92k
...N. Parker Center for Allergy and Asthma Research, the world's leading scientists, physician... ...and retaining participants in long-term clinical trials. Oversee data management for... ...potentially including hiring, preparing or assisting with the preparation of performance evaluations...Contract workWork at officeLocal area$35 - $37 per hour
...Description # Home # Search Jobs # Job Description Clinical Research Coordinator (Oncology) Contract: Palo Alto, California, US Salary Range: 35.00 - 37.00 | Per Hour Job Code: 371854 End Date: 2026-10-23 Days Left: 29 days,...Hourly payContract workTemporary work- ...Description Palo Alto Veterans Institute for Research (PAVIR is looking for a full-time Clinical Research Coordinator I . The Research Coordinator is responsible for... ...medical histories, and research assessments. Assist with specimen collection, processing, storage,...Full timeTemporary workWork at office
- Stanford University’s Department of Anesthesiology, Perioperative and Pain Medicine seeks a Clinical Research Coordinator Associate to support pediatric pain research efforts. The role involves coordinating moderately complex clinical studies and serving as a primary liaison...
- Experience with University research policies and procedures. Candidates... ...capacity to set priorities, coordinate multiple assignments, work... ...two years of experience in clinical research, or an equivalent... ...hiring, preparing or assisting with the preparation of performance...Contract workWork at officeWork from homeNight shift
- ...Description Palo Alto Veterans Institute for Research (PAVIR) supports the nation's second... ...and is looking for a full-time Clinical Research Coordinator. The Clinical Research Coordinator... ...and hospital research administration;Assist in budget management.Use R/RStudio and...Full timeTemporary workWork at office
- ...Purpose: Perform duties related to the coordination of clinical studies. Coordinate moderately complex... ...: Serve as primary contact with research participants, sponsors, and regulatory... ...participants according to protocol. Assist in developing recruitment strategies....Full timeTemporary workPart timeWork experience placementWork at officeImmediate startRemote workShift workNight shift
- ...medicine as well as cutting edge research, encompassing a wide spectrum... ...in basic, translational, clinical, health services and medical... ...seeking a Clinical Research Coordinator Associate (Fixed-term 2 years... ...participants according to protocol. Assist in developing recruitment...Fixed term contractWork experience placementWork at officeNight shift
- The Ashley Lab at Stanford University is seeking a Clinical Research Coordinator Associate to coordinate the recruitment of athletes for the collection... ...responsibilities will include recruiting, screening, assisting in the informed consent process and enrolling subjects in...Work experience placementWork at officeWork from homeNight shift
- ...The Clinical Research Coordinator Associate is responsible for the overall management and implementation of an assigned set of multiple research... ...protocol and complete annual protocol renewals. Recruit, screen, assist in the informed consent process and enroll subjects in...Local areaAfternoon shift
$160k - $170k
...grow and develop their skills.The Sr. Clinical Trial Manager (Sr CTM) is responsible for... ...out of PDs if applicable. Provides any assistance with findings from Protocol Deviation... ...data and EDC metrics reporting. Assist in coordinating study specific training or re-training...Full timeTemporary workWork experience placementWork at officeRemote workFlexible hours$125k - $170k
...Clinical Project ManagerAt Alto Neuroscience, you will play a pivotal role in advancing precision psychiatry and improving how mental... ...experienceDemonstrated knowledge of multiple aspects of clinical research operationsData-driven mindset with experience using metrics and...- ...Stanford University's Department of Orthopaedic Surgery, Spine Division is seeking a highly motivated and experienced Clinical Research Coordinator 2 (CRC2) to support the research program. This position plays a central and independent role in managing all aspects of PI...Night shift
$140k - $185k
...Clinical Trial ManagerAt Alto Neuroscience, you will play a pivotal role in advancing precision psychiatry and improving how mental health... ...representative processes), and potential serious breaches or research misconduct.Partner with Data Management to drive data entry and...Interim roleImmediate startRemote work$146k - $161k
...Clinical Trial Manager/Senior Clinical Trial ManagerWaltham, Massachusetts, United StatesOruka Therapeutics (Nasdaq: ORKA) is developing... ...team ensuring appropriate alignment, risk management and coordination across all participating functions.Successfully interface with...Work at officeRemote work3 days per week- 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. This position is hybrid and requires...Work at office
- Stanford University’s Dermatology Department is seeking an experienced Clinical Research Coordinator Associate (CRCA) to coordinate moderately complex aspects of clinical studies. The CRCA will work under the direction of the PI and clinical research manager and support...
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