Clinical Research Coordinator Associate
$34.56 - $40.3 per hourStanford
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 natural history studies, and other PI-initiated projects dealing with adult neuro-Oncology treatments. The CRCA will coordinate moderately complex aspects of two or more clinical studies and work under the close direction of the manager, senior coordinator, and principal investigator. The CRCA will manage data, enroll and follow patients on trial and assist with regulatory and financial requirements of the trials. We are seeking candidates with excellent both written and verbal communication skills and able to follow through with specifically assigned deliverables. There are opportunities for long term growth within the team, or the position can be a launching pad for a career in the biomedical sciences. This CRCA position is a full-time position, and a commitment of at least two years is required. CRCAs are expected to be available on site for up to 5 days a week. This position may require occasional evening and weekend hours.
Interested candidates, please apply with your resume and a cover letter. Please describe your background, interests, and future goals in the cover letter.
Duties Include:
- Serve as the primary contact with research participants, sponsors, and regulatory agencies.
- 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.
- Schedule subjects for appointments; contact participants with reminders or other requirements.
- Perform clerical duties in the preparation of regulatory documents and maintenance of study regulatory binder.
- Maintain subject study binders, including all forms and documents, (i.e. source data, consent forms, and master subject logs). File all appropriate correspondence.
- Extract data from source documents and complete case report forms and electronic data capture (EDC) forms for assigned studies. Resolve database queries as required.
- Collect, process and ship specimens in accordance with clinical protocol and IRB.
- Assemble study kits for study visits and order study supplies as needed.
- Prepare, administer, and score study questionnaires and tests as assigned. Perform quantitative review of forms, tests, and other measurements for completeness and accuracy.
- Participate in monitoring visits and regulatory audits.
* Other duties may also be assigned.
DESIRED QUALIFICATIONS:
- Bachelor's degree in the fields of Biology, Psychology or Neurosciences.
- Experience working with databases such as REDCap and Oncore.
- Experience processing and shipping samples.
- Have the necessary patience and resourcefulness to interact well with individuals and their families.
- Knowledge of data-related research and presentation of research data.
- Enjoy working directly with patients and their families.
- Is exceptionally organized and can balance multiple projects at one time.
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.
- Strong oral and written communication skills.
- Proficiency with Microsoft Office.
- Knowledge of medical terminology.
CERTIFICATIONS & LICENSES:
Society of Clinical Research Associates or Association of Clinical Research Professionals certification is preferred.
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:
Occasional evening and weekend hours and overtime as required.
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.
The expected pay range for this position is $34.56 to $40.30 per hour.
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.
At Stanford University, base pay represents only one aspect of the comprehensive rewards package. The Cardinal at Work website provides detailed information on Stanford's extensive range of benefits and rewards offered to employees. Specifics about the rewards package for this position may be discussed during the hiring process.
Consistent with its obligations under the law, the University will provide reasonable accommodations to applicants and employees with disabilities. Applicants requiring a reasonable accommodation for any part of the application or hiring process should contact Stanford University Human Resources.
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 orientation, gender identity, national origin, disability, protected veteran status, or any other characteristic protected by law.
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.
Stanford- ...Job Description Cancer Clinical Research Coordinator Associate - GI Oncology - Hybrid The Stanford Cancer Institute (SCI) is one of an elite number of National Cancer Institute-Designated Comprehensive Cancer Centers in the country, and is a prominent, dynamic, growing...SuggestedWork at officeAfternoon shift
$34.56 - $40.3 per hour
...Job Description Stanford University’s Department of Dermatology is seeking a Clinical Research Coordinator Associate (CRCA) to perform duties related to the coordination of clinical studies The CRCA will coordinate moderately complex aspects of one or more clinical...SuggestedHourly payWork experience placementWork at officeAfternoon shift3 days per week$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...SuggestedFull timeContract workWork at officeMonday to FridayAfternoon shift- ...Clinical Research Coordinator We are seeking a Clinical Research Coordinator to support the day-to-day coordination of clinical research studies... ..., and institutional guidelines. EPIC Proficiency Associate degree with 2+ years of related experience or a Bachelor'...SuggestedTemporary work
$51 - $52 per hour
...Description # Home # Search Jobs # Job Description Clinical Research Coordinator (oncology) Contract: Stanford, California, US Salary Range: 40.00 - 51.00 | Per Hour Job Code: 366013 End Date: 2026-08-23 Days Left: 23 days, 3...SuggestedHourly payContract workTemporary work$40 per hour
...Clinical Research Coordinator 2 Maxonic maintains a close and long-term relationship with our direct client. In support of their needs, we are... ...and Licenses: Society of Clinical Research Associates or Association of Clinical Research Professionals certification...Contract workWork at officeNight shift$37 - $45 per hour
...Clinical Research Coordinator-Oncology Onsite 5 Days Qualifications + MUST HAVE 2 years of experience as a Clinical Research Coordinator (CRC), preferably with complex clinical trials + MUST HAVE hands-on experience working directly with patients in a clinical research...Contract workTemporary work- ...Stanford University’s Memory Lab in the Department of Psychology seeks a full-time Social Science Research Coordinator to study memory and cognition in healthy adults. You will assist with collecting and analyzing EEG, pupillometry, and behavioral data, develop stimuli...Full time
- ...Clinical Research Coordinator A leading university is seeking a Clinical Research Coordinator to support the coordination and execution of oncology... ..., and patient safety. ~ Society of Clinical Research Associates (SOCRA) or Association of Clinical Research Professionals...Work experience placementWork at officeNight shift
- ...Clinical Research Coordinator The Clinical Trials Office in the company, in company Medicine seeks a Clinical Research Associate to perform duties related to the coordination of clinical studies. The incumbent will work with the team to ensure the safety and well-being...Work at office
- ...Clinical Research Coordinator Location: Burlingame, CA Job Type: Fulltime Responsibilities Coordinate clinical technology validation studies, leading operational planning and day-to-day management of research execution. Manage subject recruitment and...Full timeContract work
- ...F. Hoffmann-La Roche AG in the United States is seeking a Clinical Research Engagement Lead (CREL) to act as the primary partner and face of Roche Clinical Operations within the market. You will champion a ONE Roche mandate and drive clinical-view excellence across sites...
$108k - $202k
...About the Role As a Clinical Research Engagement Lead (CREL) at Roche, you will be the strategic partner and primary face of Roche Clinical Operations within your market, championing a "ONE Roche" approach to build high‑trust partnerships with clinical trial sites. Responsibilities...Local areaRemote workRelocation package- ...Purpose: Perform duties related to the coordination of clinical studies. Coordinate moderately... ...Duties: Serve as primary contact with research participants, sponsors, and... ...Licenses: Society of Clinical Research Associates or Association of Clinical Research Professionals...Temporary workWork experience placementWork at officeRemote workShift workNight shift3 days per week
$45 - $50 per hour
...Clinical Research Coordinator 1503775 ~ Hourly pay: $45-$50/hr ~ Worksite: Leading university (Palo Alto, CA 94304 - Hybrid) ~ W2 Employment, Group Medical, Dental, Vision, Life, Retirement Savings Program, PSL ~40 hours/week, 6 Month Assignment, Possible extension...Hourly payFull timeContract workTemporary workWork at office$115k - $121k
...Senior Clinical Research Associate South San Francisco, CA Our company is based on the science of our founder, Stanley Qi, one of the original... ...alongside CRO, reviewing monitoring visit reports, coordinating vendor trainings, reviewing study newsletters, and other...Local area- ...Clinical Research Associate Integrated Resources, Inc., is led by a seasoned team with combined decades in the industry. We deliver strategic... ...development of documents for site binders. Assembles and coordinates distribution of site binders. Serves as CRA back up...
- ...Rate: Negotiable Salary: NA, $1.00 Responsibilities: Excellent employment opportunity for a Clinical Research Associate in the South San Francisco area. Assists in the selection of investigational sites, negotiates grant contracts with...Contract work
$120k - $150k
Revolution Medicines is a late-stage clinical oncology company developing novel targeted... ...Operations, you will be responsible for Contract Research Organization (CRO) oversight and... ...guidance, and direction to Clinical Research Associates (CRAs) assigned to clinical studies....Full timeContract workFor contractorsInterim roleLocal area- ...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
- ...a positive impact on the lives of patients while enjoying competitive pay, comprehensive benefits, and the support of a dedicated clinical team. Required Qualifications: One year of recent experience as a Medical Laboratory Technician Valid license when needed...Temporary work
$146.54k - $189.64k
...Clinical Trials Manager We're here for one reason and one reason only – to cure cancer. Every moment is dedicated to developing treatments... ...Manager at Gilead/Kite, you will be responsible for: Coordinating and supervising all aspects of a clinical study. Monitors...Contract workFor contractorsInterim roleLocal area- ...Clinical Trial Manager The Clinical Trial Manager manages and leads the day-to-day clinical trial activities related to the development and execution of cross-functional and third-party vendor activities and deliverables. Additional responsibilities include independent...
$124k - $155k
...development, and commercialization of clinically differentiated, high-value... ...leadership of the clinical research studies to ensure delivery... ...as the central point of coordination to ensure clear roles,... ...Oversee Clinical Research Associates, CROs, central labs, and external...Full timeWork at officeRemote workWorldwide$120k - $150k
Revolution Medicines is a late-stage clinical oncology company developing novel targeted... ...Operations, you will be responsible for Contract Research Organization (CRO) oversight and... ...guidance, and direction to Clinical Research Associates (CRAs) assigned to clinical studies....Full timeContract workFor contractorsInterim roleLocal area- ...Senior Clinical Trial Manager South San Francisco, California, United States Role Summary Hands-on clinical trial leader responsible... ...tracking experience ~ Strong execution and cross-functional coordination skills ~ Comfortable in fast-paced, growth-stage environment...Contract workInterim role
- ...About the job Clinical Trial Manager Summary This is an opportunity to join a science-driven organization focused on advancing... ...or healthcare-related field. At least 4 years of clinical research experience, including a minimum of 2 years in a Clinical Trial...Interim roleWork at office
$155k - $175k
...Senior Clinical Trial Manager Sutro Biopharma, Inc. is seeking a driven and talented individual to join our Clinical Operations team... ..., California. Responsibilities: Develops, leads and coordinates clinical trial activities and manages the execution of 1 or more...- ...cross-functional alignment across Business, Data & Analytics, Clinical, Quality, Regulatory, Supply Chain, and IT teams. Support the... ...management, metadata management, and data modernization programs. Coordinate activities across business and technical teams to ensure...Local area
$85k - $140k
...than 400,000 patients worldwide. The Clinical Trial Manager (CTM) is responsible for... ...well with the HeartFlow Clinical Research staff and collaborate effectively with... ...onsite and field staff, clinical research coordinators, principal investigators, and vendors to...Remote jobWork experience placementWork at officeLocal areaWorldwideRelocationShift work
Do you want to receive more vacancies?
Subscribe and receive similar vacancies to Clinical Research Coordinator Associate. Be the first to apply!
- clinical research coordinator Stanford, CA
- clinical trials manager Stanford, CA
- clinical project manager Stanford, CA
- neuroscience clinical research coordinator Stanford, CA
- on-site clinical research associate (traveling/remote) Stanford, CA
- clinical trials Stanford, CA
- clinical research Stanford, CA
- clinical research physician Stanford, CA
- clinical research regulatory Stanford, CA
- clinical research coordinator

