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Crc Jobs (NOW HIRING)

SAFER Foundation

CRC II

Chicago, IL

$23.77/hr

Under the direction of the Chief of Security, the CRC II at the North Lawndale Adult Transition Center will supervise and coordinate the activities of assigned CRC I staff ensuring proper security ...

Minneapolis Heart Institute Foundation

CRC I

Minneapolis, MN · On-site

$24 - $32/hr

CRC's assist with documentation for Institutional Review Board (IRB)submissions, recruit and screen study participants and help facilitate their continued participation; abstract data from electronic ...

CRC Group

Technical Data Steward

Charlotte, NC · On-site

At CRC Group, we're committed to supporting every aspect of teammates' well-being - physical, emotional, financial, social, and professional. Our best-in-class benefits program is designed to care ...

Safer Foundation

CRC II

Chicago, IL · On-site

Under the direction of the Chief of Security, the CRC II at the North Lawndale Adult Transition Center will supervise and coordinate the activities of assigned CRC I staff ensuring proper security ...

CRC Group

Scrum Master/Project Manager

Charlotte, NC · On-site

$50.25 - $67.25/hr

Enables Agile teams to realize value by facilitating Agile ceremonies, following CRC Group's Best Practices, removing impediments, coaching on Agile processes. ESSENTIAL DUTIES AND RESPONSIBILITIES ...

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How much do crc jobs pay per hour?

As of Aug 12, 2026, the average hourly pay for crc in the United States is $27.22, according to ZipRecruiter salary data. Most workers in this role earn between $21.15 and $29.57 per hour, depending on experience, location, and employer.

What are the key skills and qualifications needed to thrive as a clinical research coordinator, and why are they important?

To thrive as a Clinical Research Coordinator, you need a solid background in life sciences, clinical research protocols, and regulatory compliance, often supported by a bachelor's degree in a health-related field. Familiarity with clinical trial management systems (CTMS), electronic data capture (EDC) tools, and certifications such as CCRC or ACRP are commonly required. Strong organizational skills, attention to detail, and effective communication help build trust with patients and ensure smooth coordination among research teams. These competencies are crucial for maintaining study integrity, regulatory adherence, and successful trial outcomes.

What is the difference between Crc vs Coder?

AspectCrcCoder
CertificationsCertified Rehabilitation Counselor (CRC) certificationNo specific certification required, but coding certifications like CPC or CCS are common
Work EnvironmentHealthcare, rehabilitation centers, mental health facilitiesHealthcare, medical offices, hospitals, or outpatient clinics
Industry UsageRehabilitation and mental health servicesMedical billing, documentation, and health information management
Job FocusPatient counseling, rehabilitation planningMedical coding, data entry, billing

The main difference between a Crc and a Coder is their focus and certification. Crcs are trained to provide rehabilitation counseling and typically hold specific credentials, working mainly in healthcare and mental health settings. Coders, on the other hand, focus on translating medical records into codes for billing and documentation, often without requiring formal certification. Both roles are essential in healthcare but serve different functions and require different skill sets.

What are the duties of a CRC?

A CRC (Clinical Research Coordinator) is responsible for managing clinical trials, recruiting and consenting participants, collecting and recording data, ensuring compliance with protocols and regulations, and coordinating with research teams. They often use specialized software and must adhere to Good Clinical Practice (GCP) standards. Strong organizational and communication skills are essential for this role.

What is a clinical research coordinator?

Clinical Research Coordinators (CRCs) are professionals who oversee and manage clinical trials and research studies conducted in medical settings. They are responsible for coordinating daily activities, ensuring compliance with protocols, recruiting and enrolling participants, and maintaining accurate records. CRCs work closely with principal investigators, sponsors, and regulatory bodies to ensure that studies are conducted ethically and efficiently. Their role is crucial in advancing medical knowledge and patient care through research.

How does a clinical research coordinator typically collaborate with investigators and study sponsors during a clinical trial?

A Clinical Research Coordinator (CRC) plays a key role in facilitating communication between investigators, study sponsors, and other research staff. CRCs are responsible for ensuring that the study protocol is followed, collecting and managing data, and coordinating patient visits. They often schedule meetings, report progress, handle regulatory documentation, and address queries from sponsors or monitors. This requires strong organizational and interpersonal skills to keep all parties aligned and the study running smoothly.
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CRC jobs near you
Infographic showing various Crc job openings in the United States as of August 2026, with employment types broken down into 1% As Needed, 74% Full Time, 23% Part Time, 1% Temporary, and 1% Contract. Highlights an 93% Physical, 2% Hybrid, and 5% Remote job distribution, with an average salary of $56,615 per year, or $27.2 per hour.

Clinical Research Coordinator (CRC)

Smarter HR Solutions LLC

Orange, CA

$90K - $100K/yr

Full-time

Re-posted 11 days ago

Job description

Job description
Job Title: Clinical Research Coordinator (CRC)
Job Type: Full-Time
Job Location(s): Orange, CA *This role is ONSITE*
Job Salary: $32-$35/hour ($66,560.00 - $72,800.00 per year)
Job Schedule: M-F 40-hours/week

This is an on-site position in Orange, CA, and applicants must reside within a commutable distance of 50 miles or less or be able to independently relocate. THIS IS NOT A REMOTE POSITION.


Position Summary

The Clinical Research Coordinator will support the planning, execution, and closeout of clinical studies involving human subjects. This includes FDA-regulated drug and device trials, NIH-funded research, and investigator-initiated protocols. The CRC ensures compliance with California-specific regulatory frameworks, institutional policies, and federal guidelines (FDA, ICH-GCP, HIPAA).


Experience in CRC in Liver/GI/Obesity studies preferred!

Key Responsibilities

Study Operations

  • Coordinate Phase I–IV clinical trials across multiple therapeutic areas.
  • Prepare IRB submissions, amendments, and continuing reviews.
  • Develop and maintain study documentation, SOPs, and case report forms.
  • Schedule and conduct study visits, collect data, and ensure protocol adherence.

Participant Management

  • Recruit, screen, and consent participants in accordance with CPHS and institutional HRPP standards
  • Educate participants on study procedures, risks, and rights
  • Monitor for adverse events and report per FDA and California Health & Safety Code §24170–24179.5

Regulatory & Compliance

  • Maintain audit-ready records and ensure GCP compliance
  • Handle protected health information (PHI) securely under California law
  • Liaise with sponsors, monitors, and regulatory bodies

Data & Budget Oversight

  • Enter and validate data in CTMS and EDC systems
  • Assist with budget development and financial tracking
  • Coordinate biospecimen collection, processing, and shipping

Job Type: Full-time

Work Location: In person



Requirements
Qualifications

Education

  • Bachelor’s degree in health sciences, biology, nursing, or related field (Master’s preferred).
  • Formal training in clinical research or regulatory affairs.


Experience
  • 1–3 years of clinical research coordination experience, primarily in liver/GI/obesity studies.
  • Familiarity with California IRB systems and CPHS protocols.
  • Experience with FDA-regulated trials and NIH-funded studies.


Skills
  • Strong organizational and time management abilities.
  • Excellent verbal and written communication skills.
  • Proficiency in CTMS, EDC, and IRB platforms (e.g., iRIS, OnCore).
  • Ability to work independently and collaboratively across teams
  • Preferably bilingual in English/Spanish