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Crca Jobs (NOW HIRING)

PFS Billing Rep, FT, Days

Greenville, SC · On-site

$16.75 - $21.75/hr

CRCA or CRCR - preferred Knowledge, Skills and Abilities * Facility claims and billing follow up and/or medical office experience * Communication skills and respect for details - preferred. Work ...

Review Assessable Units and Assessable Categories (AUACs) and assist teams in completing CRCA questionnaires; identify and challenge Major Change Events that impact responses. * Prepare materials for ...

PFS Billing Rep, FT, Days

Greenville, SC

$16.75 - $21.75/hr

CRCA or CRCR - preferred Knowledge, Skills and Abilities * Facility claims andbilling follow up and/or medical office experience * Communication skills and respect for details - preferred. Work Shift ...

Review Assessable Units and Assessable Categories (AUACs) and assist teams in completing CRCA questionnaires; identify and challenge Major Change Events that impact responses. * Prepare materials for ...

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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 (24-Month Fixed-Term)

Clinical Research Coordinator Associate (24-Month Fixed-Term)

Stanford University

Stanford, CA

$28.50 - $38/hr

Other

Posted 14 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

The Division of Child Neurology is seeking a Clinical Research Coordinator Associate (CRCA) to coordinate a variety of new and ongoing pediatric neurology clinical research projects. The Clinical Research Coordinator is responsible for the overall management and implementation of an assigned set of multiple research protocols assuring efficiency and regulatory compliance. These studies will be conducted at the Stanford Hospital and Clinics.  He/she will work as part of a clinical trials research team and report to various Principal Investigators conducting clinical research. Responsibilities include preparation of initial study documents for IRB submission in compliance with all local, state and federal regulations; advise the IRB of amendment changes to the protocol and complete annual protocol renewals. Recruit, screen, assist in the informed consent process and enroll subjects in accordance with good clinical practice guidelines. Collect, record and maintain complete data files using good clinical practice in accordance to HIPAA regulations. He/she participates in data retrieval, reporting, and preparation of files and Case Report Forms for the various studies.  The successful candidate will interact with subjects by scheduling diagnostic and research evaluation visits, perform study related assessments including collection of blood samples, processing and shipment. Maintain drug accountability, adequate study supplies and equipment. The coordinator will oversee subject compliance to the study protocol, obtain information from the study subject regarding any changes in their medications or adverse events and promptly report the findings to physicians for documentation in the subject's medical record. Report all serious adverse events promptly to investigators, sponsors and the IRB. Protect the rights, safety and well-being of human subjects involved in the clinical trials.  


Duties include*:

  • Serve as primary contact with research participants, sponsors, and regulatory agencies.  Coordinate studies from startup 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.

* - Other duties may also be assigned.


 

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:

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.

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 the salary or hourly wage the university reasonably expects to pay for a position upon hire. 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 Stanfords 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: Fixed-Term
  • Grade: F
  • Requisition ID: 109311
  • Work Arrangement : On Site

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