Clinical Research Coordinator Associate - ID/Gilead
$61k - $76kDev
Clinical Research Coordinator Associate - ID/Gilead Full-time Jobs for Humanity is partnering with Stanford University to build an inclusive and just employment ecosystem. Therefore, we prioritize individuals coming from the following communities: Refugee, Neurodivergent, Single Parent, Blind or Low Vision, Deaf or Hard of Hearing, Black, Hispanic, Asian, Military Veterans, the Elderly, the LGBTQ, and Justice Impacted individuals. This position is open to candidates who reside in and have the legal right to work in the country where the job is located. Company Name: Stanford University The Stanford Center for Clinical Research (SCCR) is a growing academic research organization within the Stanford Department of Medicine. Our mission is to conduct and promote high-impact, innovative clinical research to improve human health. At SCCR, we strive to find team members who are passionate about their work, flexible, fun, and want to deliver results. We place a high priority on equipping our staff to perform their job efficiently, helping them acquire new skills and grow within the organization. We encourage our team to have a healthy balance between work commitments and life outside of work and provide support to achieve this balance. If you are looking to make a large impact through global-reaching clinical research, we encourage you to apply! In collaboration with the Division of Infectious Diseases and others at Stanford, SCCR is seeking 2 Clinical Research Coordinator Associates (CRCAs) to work on a highly impactful COVID-19 study, including but not limited to treatment trial for COVID-19. The CRCAs will work under a CRCII to recruit and enroll participants and monitor research participant workflow to ensure study visit completion. The CRCAs will coordinate all aspects of the study visits and work in a dynamic atmosphere and as part of a large team in a supportive environment. There will be the opportunity to work closely with fellow coordinators and research assistants, physicians, nurses, and technicians. Direct patient contact is a primary responsibility of these roles. The CRCAs are required to have the ability to multi-task in a high-energy environment. A flexible work schedule, outstanding communication and organizational skills, and attention to detail are required in successful candidates. The CRCAs will act as point of contacts for participants and staff, present at meetings and huddles, and troubleshoot research related issues. The CRCAs will be responsible for ensuring compliance with federal, state, local, and sponsor regulations and work under the direction of their supervisor/s. The CRCAs will work under close direction of the principal investigator and/or study coordinator/supervisor. Other duties may also be assigned. This is an on-site position. Duties include: Serve as primary contact with research participants, sponsors, and regulatory agencies. Coordinate studies from start-up through close-out. Determine eligibility of and gather consent from study participants according to protocol. Assist in developing recruitment strategies. Coordinate collection of study specimens and processing. Collect and manage patient and laboratory data for clinical research projects. Manage research project databases, develop flow sheets and other study related documents, and complete study documents/case report forms. Ensure compliance with research protocols, and review and audit case report forms for completion and accuracy with source documents. Prepare regulatory submissions, and ensure Institutional Review Board renewals are completed. Assemble study kits for study visits, monitor scheduling of procedures and charges, coordinate documents, and attend monitoring meetings with sponsors, acting as primary contact. Monitor expenditures and adherence to study budgets and resolve billing issues in collaboration with finance and/or management staff. Interact with the principal investigator regularly, ensuring patient safety and adherence to proper study conduct. Ensure essential documentation and recording of patient and research data in appropriate files per institutional and regulatory requirements. Participate in monitor visits and regulatory audits. The job duties listed are typical examples of work performed by positions in this job classification and are not designed to contain or be interpreted as a comprehensive inventory of all duties, tasks, and responsibilities. Specific duties and responsibilities may vary depending on department or program needs without changing the general nature and scope of the job or level of responsibility. Employees may also perform other duties as assigned.
DESIRED QUALIFICATIONS:
Clinical research operations certificate or interest in working toward one. Valid CA driver's license.EDUCATION & EXPERIENCE (REQUIRED):
Two-year college degree and two years related work experience or a Bachelor's degree in a related field or an equivalent combination of related education and relevant experience.KNOWLEDGE, SKILLS AND ABILITIES (REQUIRED):
Strong interpersonal skills. Proficiency with Microsoft Office. Knowledge of medical terminology.CERTIFICATIONS & LICENSES:
Working toward certification(s) to perform basic patient measurements and tests, such as phlebotomy and EKG.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.WORKING 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, The expected pay range for this position is $61,000 to $76,000 per annum. Stanford University provides pay ranges representing its good faith estimate of what the university reasonably expects to pay for a position. The pay offered to a selected candidate will be determined based on factors such as (but not limited to) the scope and responsibilities of the position, the qualifications of the selected candidate, departmental budget availability, internal equity, geographic location and external market pay for comparable jobs. Why Stanford is for You Imagine a world without search engines or social platforms. Consider lives saved through first-ever organ transplants and research to cure illnesses. Stanford University has revolutionized the way we live and enrich the world. Supporting this mission is our diverse and dedicated 17,000 staff. We seek talent driven to impact the future of our legacy. Our culture and unique perks empower you with: Freedom to grow . We offer career development programs, tuition reimbursement, or audit a course. Join a TedTalk, film screening, or listen to a renowned author or global leader speak. A caring culture . We provide superb retirement plans, generous time-off, and family care resources. A healthier you . Climb our rock wall, or choose from hundreds of health or fitness classes at our world-class exercise facilities. We also provide excellent health care benefits. Discovery and fun . Stroll through historic sculptures, trails, and museums. Enviable resources . Enjoy free commuter programs, ridesharing incentives, discounts and more. Stanford is an equal employment opportunity and affirmative action employer. All qualified applicants will receive consideration for employment without regard to race, color, religion, sex, sexual orien #J-18808-Ljbffr Dev- Job-ID: 201373Category: ResearchLocation: Stanford, CA, United StatesWorkplace: HybridContract: RegularPosted: 2026... ...the Stanford University School of Medicine is seeking a Clinical Research Coordinator Associate to perform duties related to the coordination of clinical...SuggestedPart timeWork experience placementWork at officeWork from homeNight shift
$34.56 - $40.3 per hour
Cancer Clinical Research Coordinator Associate - Melanoma (Hybrid) The Stanford Cancer Institute (SCI) is one of only 49 National Cancer Institute (NCI)... ...: 1013 Employee Status: Regular Grade: F Requisition ID: 107721 Work Arrangement : Hybrid Eligible #J-18808-Ljbffr...SuggestedHourly payFull timeWork experience placementInternshipWork at office$31.84 - $37.79 per hour
Clinical Research Coordinator Associate | Stanford University job at Stanford University. Stanford, CA. The Stanford Center for Precision Mental Health... ...Code: 1013 Employee Status: Regular Grade: F Requisition ID: 106016 Work Arrangement : On Site #J-18808-Ljbffr Stanford...SuggestedHourly payFull timeWork experience placementWork at officeImmediate startAfternoon shift$34.56 - $40.3 per hour
Overview Clinical Research Coordinator Associate (1 Year Fixed-Term) Department: School of Medicine, Redwood City, California, United States. The Department... ...013 Employee Status: Fixed-Term Grade: F Requisition ID: 107271 Work Arrangement: On Site #J-18808-Ljbffr...SuggestedHourly payFull timeFixed term contractWork experience placementWork at officeAfternoon shift- ...oriented English/Spanish bilingual Full-Time Research Coordinator / Research Data Collector for a... ...manage patient and laboratory data for clinical research projects. Manage research... ...RequiredSociety of Clinical Research Associates or Association of Clinical Research Professionals...SuggestedFull timeWork experience placementWork at officeNight shiftWeekend workAfternoon shift
- ...critical care medicine as well as cutting edge research, encompassing a wide spectrum of programs in basic, translational, clinical, health services and medical education.... ...Medicine is seeking a Clinical Research Coordinator Associate (Fixed-term 2 years) to perform duties...Fixed term contractWork experience placementWork at officeNight shift
- ...Clinical Research Coordinator Associate Stanford University's Department of Dermatology is seeking an experienced Clinical Research Coordinator Associate (CRCA) to perform duties related to the coordination of clinical studies. The CRCA will coordinate moderately complex...Work experience placementWork at officeAfternoon shift3 days per week
- A prestigious research institution is seeking an Assistant Clinical Research Coordinator Associate to support multiple clinical research studies. This role involves assisting with study coordination, data collection, and ensuring regulatory compliance. Ideal candidates...
- ...medicine. The department also conducts cutting‑edge research encompassing basic, translational, clinical, health services, and medical education programs... ...The department is seeking a Clinical Research Coordinator Associate for a fixed‑term 2‑year position. The Associate...Fixed term contractWork experience placementWork at officeAfternoon shift
- The Stanford University School of Medicine, Department of Surgery, Division of Vascular Surgery, seeks a Clinical Research Coordinator Associate to coordinate clinical studies on the Stanford campus in a hybrid on-site/remote arrangement. Under the Principal Investigators...Remote work
- ...The Department of Surgery, Division of Vascular Surgery at the Stanford University School of Medicine is seeking a Clinical Research Coordinator Associate to perform duties related to the coordination of clinical studies. The CRCA will coordinate moderately complex aspects...Work from home
- Stanford University Department of Cardiothoracic Surgery, Division of Thoracic Surgery is seeking a Clinical Research Coordinator Associate to perform duties related to the coordination of clinical studies. The individual will coordinate moderately complex aspects of at...Afternoon shift
$34.56 - $40.3 per hour
...with cancer‑relevant expertise from four Schools and over 30 departments across Stanford University. We seek a Cancer Clinical Research Coordinator Associate to help us enact our mission to reduce cancer mortality through comprehensive programs of cancer research,...Hourly payWork experience placementWork at officeAfternoon shift- Stanford University’s Stanford Center for Clinical Research (SCCR) seeks two Clinical Research Coordinator Associates to support a high-impact COVID-19 study. You will coordinate visits, screen eligibility, obtain consent, collect specimens, and manage data under supervision...
- ...Competitive full time salary. Excellent Stanford benefits. The Neuromuscular Division of Neurology is seeking a clinic Clinical Research Coordinator Associate (CRCA) to coordinate the oversight and implementation of research protocols assuring efficiency and regulatory...Full timeWork experience placementWork at officeAfternoon shift
- Stanford University School of Medicine seeks a Clinical Research Coordinator Associate (fixed-term 2 years) to coordinate perioperative clinical studies, including EEG/MRI data collection and neuropsychological testing. Responsibilities include participant consent, regulatory...Fixed term contract
- Stanford University in Stanford, CA, seeks a Clinical Research Coordinator Associate to manage multiple protocols, ensure regulatory compliance, and support IRB submissions. This on-site role works with the Stanford Hospital and Clinics, coordinating visits, data collection...
$34.56 - $40.3 per hour
...Clinical Research Coordinator Associate Stanford University's Department of Neurosurgery is seeking a Clinical Research Coordinator Associate (CRCA) to perform duties related to the coordination of clinical research studies. Studies may include drug/device trials, longitudinal...Hourly payFull timeWork experience placementWork at officeAfternoon shift$160k - $170k
...grow and develop their skills. The Sr. Clinical Trial Manager (Sr CTM) is responsible... ...and EDC metrics reporting. Assist in coordinating study specific training or re-training... ...information/informed consents and completes associated checklists as per Ascendis SOPs....Temporary workWork experience placementWork at officeRemote workFlexible hours$29.44 - $33.26 per hour
...Hepatology at Stanford University is seeking an Assistant Clinical Research Coordinator Associate (aCRC) to support 4-6 clinical research studies on-site... ...: 1012 Employee Status: Regular Grade: E Requisition ID: 107587 Work Arrangement: On Site #J-18808-Ljbffr...Hourly payFull time- Stanford University is seeking a Clinical Research Coordinator 2 to conduct clinical research and work independently on progressively more complex... ...and Licenses RequiredSociety of Clinical Research Associates or Association of Clinical Research Professionals certification...Contract workWork at officeNight shift
$38.55 - $57.83 per hour
...Office-Valley Position Overview: Collects, compiles and presents clinical data for assigned area, ensuring accuracy, timeliness and accessibility of information. Maintains clinical and/or research databases for identified programs/ specialty clinics. Collects data...Full timeWork at officeMonday to FridayShift workWeekend work$46 - $52 per hour
...Description # Home # Search Jobs # Job Description Clinical Research Coordinator Contract: Palo Alto, California, US Salary Range: 46.00 - 52.00 | Per Hour Job Code: 372081 End Date: 2026-11-13 Days Left: 29 days, 4 hours left...Hourly payContract workTemporary work$33 - $37 per hour
...Job Title: Clinical Research Data CoordinatorJob Description This role focuses on entering and validating clinical research data, maintaining... ...trials. Work closely with data providers, such as study coordinators and clinical staff, to discuss and clarify data ambiguities...Full timeContract workTemporary work$35 - $70 per hour
...Title: Clinical Research Coordinator Pay Rate Range: $35.00 - $70.00/hr (DOE, based on experience and level) Employment Type: Contract Schedule: Full-time, Monday - Friday | 8:00 AM - 5:00 PM Location: Stanford, CA 94305 Tekberry is looking for a highly...Full timeContract workWork at officeMonday to FridayAfternoon shift- ...Clinical Research Coordinator BMT Seeking a Clinical Research professional to independently manage clinical research activities, with a focus on oncology treatment trials and Phase I studies in Bone Marrow Trials (BMT). This healthcare setting role involves patient...Temporary work
$37 - $45 per hour
...Clinical Research Coordinator 2 This role leads and coordinates clinical research activities with a focus on oncology and bone marrow transplant... ...are submitted to the FDA when applicable and that all associated documentation is complete. Ensure timely completion and...Contract workTemporary workWork at office$125k - $135k
Position: On-site Clinical Research Associate Location: Newark, CAJob Id: 416 # of Openings: 0 Clinical Research AssociateAbout UsProtagonist Therapeutics is a biopharmaceutical company built on a proprietary...Full timeTemporary workWorldwideFlexible hours$135k - $150k
Position: Senior Clinical Research Associate Location: Newark, CAJob Id: 397 # of Openings: 0 Senior... ...reports) •May assist with development and coordination of any trial-specific sub-studies •Assist with...Contract workInterim roleLocal areaWorldwide- ...Assistant Clinical Research Coordinator A leading university is seeking an Assistant Clinical Research Coordinator to support the coordination and execution of clinical research studies. This role assists with participant recruitment, data collection, regulatory documentation...
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