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Crc Jobs in Kentucky (NOW HIRING)

IQVIA

Senior Research Coordinator

Versailles, KY · On-site

$44K - $110K/yr

This breadth of responsibility not only strengthens your core CRC skills but also prepares you for future roles in clinical operations, monitoring, and beyond. What You'll Gain: * Broadened Skill Set:

IQVIA

Senior Research Coordinator

Versailles, KY

$44K - $110K/yr

This breadth of responsibility not only strengthens your core CRC skills but also prepares you for future roles in clinical operations, monitoring, and beyond. What You'll Gain: * Broadened Skill Set:

IQVIA, Inc.

Senior Research Coordinator

Lexington, KY · On-site

$44K - $110K/yr

This breadth of responsibility not only strengthens your core CRC skills but also prepares you for future roles in clinical operations, monitoring, and beyond. What You'll Gain: * Broadened Skill Set:

IQVIA

Senior Research Coordinator

Lexington, KY

$44K - $110K/yr

This breadth of responsibility not only strengthens your core CRC skills but also prepares you for future roles in clinical operations, monitoring, and beyond. What You'll Gain: * Broadened Skill Set:

IQVIA

Senior Research Coordinator

Lexington, KY

$44K - $110K/yr

This breadth of responsibility not only strengthens your core CRC skills but also prepares you for future roles in clinical operations, monitoring, and beyond. What You'll Gain: * Broadened Skill Set:

Ora

Clinical Research Coordinator I

Louisville, KY · On-site

$23.25 - $31/hr

Once onsite, our CRC I's will administrate various technician-based tasks by collecting, recording, and organizing subject and research information during clinical research study visits while ...

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Crc information

See Kentucky salary details

$9

$25

$41

How much do crc jobs pay per hour?

As of Aug 15, 2026, the average hourly pay for crc in Kentucky is $25.40, according to ZipRecruiter salary data. Most workers in this role earn between $19.74 and $27.59 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.

What are the most commonly searched types of Crc jobs in Kentucky?

The most popular types of Crc jobs in Kentucky are:

What job categories do people searching Crc jobs in Kentucky look for?

The top searched job categories for Crc jobs in Kentucky are:

What cities in Kentucky are hiring for Crc jobs?

Cities in Kentucky with the most Crc job openings:

Crc jobs near you
Infographic showing various Crc job openings in Kentucky 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 $52,837 per year, or $25.4 per hour.

Clinical Research Coordinator Level 1

Baptist Health

Louisville, KY • On-site

$23.25 - $31/hr

Full-time

Re-posted 18 days ago

Baptist Health South Florida rating

8.1

Company rating: 8.1 out of 10

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Job description

Summary
Job Description:
Baptist Health is looking for a Clinical Research Coordinator I to join our team in Louisville, KY
Under limited supervision, the Clinical Research Coordinator I (CRC) coordinates patient care in compliance with local, state and federal guidelines and regulations through IRB approved protocol requirements. The CRC uses their developing and/or basic knowledge of clinical trial research along with their hospital experience to work collaboratively with individuals associated with the care and treatment of the patient. It is the expectation the CRC will utilize day-to-day experience and collaborations with senior staff to broaden their knowledge base and capabilities. They will seek out opportunities to build their knowledge of the organization, research processes and scope of work. They will understand the guidelines, regulations, and policies associated with conducting clinical trial research and use that insight to evaluate and resolve problems or seek out guidance. The CRC collaborates with the investigators, research staff and other departmental stakeholders to conduct clinical trial coordination per protocol. Through clear documentation, the CRC will define any changes in condition, adverse events, concomitant medication use, protocol compliance, and response to study intervention. The CRC works collaboratively with individuals associated with the care and treatment of the patient.
Qualifications:
  • Technical Diploma or Degree/certification must be in biology, public health, pharmacy, or health related field.
  • Oncology clinical experience, not required, but preferred for this role.
  • 3 years of experience in clinical research or as a clinical trial coordinator.
  • Proficient with a computer including navigating websites, electronic data systems, electronic medical records, Excel, Word, PowerPoint.
  • Must obtain ACLS/BLS training within 6 months

If you would like to be part of a growing family focused on supporting clinical excellence, teamwork and innovation, we urge you to apply now!
Baptist Health is an Equal Employment Opportunity employer.

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About Baptist Health South Florida

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Baptist Health South Florida is the largest healthcare organization in the region, with 12 hospitals, more than 27,000 employees, 4,000 physicians and 100 outpatient centers, urgent care facilities and physician practices spanning across Miami-Dade, Monroe, Broward and Palm Beach counties. Baptist Health has internationally renowned centers of excellence in cancer, cardiovascular care, orthopedics and sports medicine, and neurosciences. A not-for-profit organization supported by philanthropy and committed to its faith-based charitable mission of medical excellence, Baptist Health has been recognized by Fortune as one of the 100 Best Companies to Work For in America and by Ethisphere as one of the World's Most Ethical Companies.

Industry

Health care and social assistance

Company size

10,000+ Employees

Headquarters location

Miami, FL, US

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