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How much do crca jobs pay per hour?

As of Jun 6, 2026, the average hourly pay for crca in the United States is $26.34, according to ZipRecruiter salary data. Most workers in this role earn between $15.14 and $30.77 per hour, depending on experience, location, and employer.

What are the key skills and qualifications needed to thrive in the Crca position, and why are they important?

To succeed as a Clinical Research Coordinator Associate (CRCA), you should have a background in life sciences or a related field, strong organizational skills, and attention to detail. Familiarity with clinical trial protocols, regulatory compliance software, and Good Clinical Practice (GCP) certification are highly valued. Excellent interpersonal skills, effective communication, and the ability to multitask set top performers apart. These skills ensure accurate study execution, regulatory compliance, and strong collaboration within multidisciplinary research teams.

What does a typical day look like for a CRCA?

A typical day for a CRCA involves coordinating clinical trial activities, such as recruiting and consenting participants, collecting and managing study data, and ensuring adherence to study protocols. You may spend part of your day communicating with principal investigators, scheduling appointments, and maintaining accurate clinical records. Collaboration with research nurses, data managers, and regulatory staff is a key component of the role. This position often requires balancing multiple projects and deadlines, making organizational and time management skills crucial. Working as a CRCA offers a dynamic environment with opportunities to learn from experienced researchers and contribute directly to advancing medical knowledge.

What is a CRCA job?

A CRCA (Clinical Research Coordinator Associate) is responsible for assisting in the management and coordination of clinical research studies. They help ensure compliance with regulatory guidelines, collect and document data, and support researchers, participants, and clinical staff. CRCAs also assist with scheduling visits, maintaining study records, and preparing reports. Their role is critical in ensuring that clinical trials are conducted efficiently and ethically.

More about Crca jobs
What states have the most Crca jobs? States with the most job openings for Crca jobs include:
Clinical Research Coordinator Associate

Clinical Research Coordinator Associate

Stanford University

Stanford, CA

$28.50 - $38/hr

Other

Posted 12 days ago


Stanford University rating

7.8

Company rating: 7.8 out of 10

Based on 24 frontline employees who took The Breakroom Quiz

192nd of 532 rated colleges and universities


Job description

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, http://adminguide.stanford.edu.

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 (https://cardinalatwork.stanford.edu/benefits-rewards) 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 by submitting a contact form.

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.
 

Additional Information
  • Schedule: Full-time
  • Job Code: 1013
  • Employee Status: Regular
  • Grade: F
  • Requisition ID: 107631
  • Work Arrangement : On Site

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