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Cra Jobs in Kentucky (NOW HIRING)

Solomon Page

Contract CRA

Covington, KY · On-site

$90 - $100/hr

We are seeking an experienced and highly motivated Clinical Research Associate (CRA) to support a Phase 3 clinical trial in the Kidney transplant therapeutic area. The ideal candidate will have a ...

Solomon Page

Contract CRA

Covington, KY · On-site

$90 - $100/hr

We are seeking an experienced and highly motivated Clinical Research Associate (CRA) to support a Phase 2 clinical trial in the lung transplant therapeutic area. The ideal candidate will have a ...

IQVIA

CRA 1, IQVIA Biotech

Lexington, KY

$71K - $145K/yr

IQVIA Biotech is now hiring for CRA 1 with a minimum of 6 months of on-site monitoring. Must have experience monitoring in oncology solid tumor. IQVIA Biotech is a full-service CRO purpose-built to ...

IQVIA

CRA 1, IQVIA Biotech

Lexington, KY

$71K - $145K/yr

IQVIA Biotech is now hiring for CRA 1 with a minimum of 6 months of on-site monitoring. Must have experience monitoring in oncology solid tumor. IQVIA Biotech is a full-service CRO purpose-built to ...

CTI

Clinical Trial Manager

Covington, KY · On-site +1

Develop CRA tools and CRA training materials * Organize and conduct CRA meetings/calls if in project scope * Ensure accurate tracking of any relevant study information related to Clinical Monitoring ...

CTI

Clinical Trial Manager

Covington, KY · Remote

Develop CRA tools and CRA training materials * Organize and conduct CRA meetings/calls if in project scope * Ensure accurate tracking of any relevant study information related to Clinical Monitoring ...

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Cra information

See Kentucky salary details

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How much do cra jobs pay per hour?

As of Aug 8, 2026, the average hourly pay for cra in Kentucky is $35.72, according to ZipRecruiter salary data. Most workers in this role earn between $25.05 and $45.72 per hour, depending on experience, location, and employer.

What is the job of a clinical research associate?

A clinical research associate (CRA) is responsible for monitoring clinical trials to ensure they are conducted according to protocols, Good Clinical Practice (GCP), and regulatory requirements. They oversee site activities, verify data accuracy, and coordinate communication between investigators and sponsors to ensure trial integrity and compliance.

What is a CRA?

A CRA, or clinical research associate, is an investigator who makes sure that medical research follows protocols and meets ethical standards. The primary responsibilities of CRAs include monitoring clinical research trials to verify the accuracy of the trial data as well as the safety and well-being of patients. To carry out these duties, CRAs visit the clinical sites where a study takes place, such as hospitals and other facilities, review documents, and observe trial proceedings.

What are the key skills and qualifications needed to thrive as a Chartered Accountant (CA), and why are they important?

To thrive as a Chartered Accountant, you need a strong background in accounting principles, financial analysis, and auditing, typically supported by a recognized CA or equivalent accounting certification. Expertise in accounting software such as SAP, QuickBooks, or Oracle, as well as proficiency in Excel and relevant tax systems, is often required. Attention to detail, analytical thinking, and integrity are crucial soft skills for ensuring accuracy and ethical financial reporting. These skills and qualifications are vital for maintaining regulatory compliance, supporting business decisions, and upholding stakeholder trust.

What qualifications do I need to be a clinical research associate?

To become a clinical research associate (CRA), candidates typically need a bachelor's degree in life sciences, health sciences, or a related field. Relevant experience in clinical trials, knowledge of Good Clinical Practice (GCP) guidelines, and strong organizational skills are also important; some roles may require certification such as the Association of Clinical Research Professionals (ACRP) or Society of Clinical Research Associates (SoCRA) credentials.

Is it hard to get a clinical research associate job?

Securing a clinical research associate (CRA) position can be competitive, often requiring a relevant degree in life sciences or healthcare, along with experience in clinical trials. Certifications like the CCRA or RAC can improve job prospects, and familiarity with regulatory guidelines and trial management tools is beneficial.

How does a CRA typically collaborate with site staff and sponsors during a clinical trial?

A CRA serves as a vital link between the clinical trial sponsor and the investigational site staff. They regularly communicate with site personnel to ensure compliance with study protocols, resolve issues, and verify data accuracy. CRAs also coordinate with sponsors by providing updates, reporting findings, and facilitating site visits. This collaboration helps maintain high-quality standards and ensures that trials progress smoothly and according to regulatory guidelines.

What is the difference between Cra vs Clinical Research Associate?

AspectCraClinical Research Associate
CredentialsTypically requires a degree in life sciences or related field; certifications like CCRP or RAC are commonSame as Cra, often holds certifications like CCRP or RAC
Work EnvironmentWorks on clinical trial sites or in offices, monitoring study progressMonitors clinical trials, manages site compliance, and ensures protocol adherence
Employer & IndustryPharmaceutical companies, CROs, biotech firmsPharmaceutical companies, CROs, biotech firms

The term Cra is often used interchangeably with Clinical Research Associate, as both roles involve monitoring clinical trials, ensuring compliance, and working within the same industry. The main difference is that Cra is a broader abbreviation, while Clinical Research Associate is the full job title. Both require similar credentials and work environments, making them essentially the same role described differently.

More about Cra jobs
What are the most commonly searched types of Cra jobs in Kentucky? The most popular types of Cra jobs in Kentucky are:
What are popular job titles related to Cra jobs in Kentucky? For Cra jobs in Kentucky, the most frequently searched job titles are:
What job categories do people searching Cra jobs in Kentucky look for? The top searched job categories for Cra jobs in Kentucky are:
What cities in Kentucky are hiring for Cra jobs? Cities in Kentucky with the most Cra job openings:
What are popular job titles related to Cra jobs in KY? For Cra jobs in KY, the most frequently searched job titles are:
Cra jobs near you
Infographic showing various Cra job openings in Kentucky as of August 2026, with employment types broken down into 88% Full Time, 7% Part Time, 1% Temporary, and 4% Contract. Highlights an 83% Physical, 4% Hybrid, and 13% Remote job distribution, with an average salary of $74,295 per year, or $35.7 per hour.

Contract CRA

Solomon Page

Covington, KY • On-site

$90 - $100/hr

Contractor

Medical, Dental, Vision, Retirement

Re-posted 15 days ago

Job description

We are seeking an experienced and highly motivated Clinical Research Associate (CRA) to support a Phase 3 clinical trial in the Kidney transplant therapeutic area. The ideal candidate will have a strong background in site monitoring and clinical trial management, with direct experience supporting pulmonary or transplant studies. This is a home-based position for a CRA located in the Midwest/Central U.S. region, with regular travel to assigned investigative sites across the United States.
  • Location: Midwest/Central United States (Home-Based)
  • Employment Type: 1.0 FTE Contract
  • Contract Duration: 6 Months with Possibility of Extension
  • Start Date: ASAP
  • Therapeutic Area: Kidney Transplant
  • Clinical Trial Phase: Phase III
  • Pay Rate: $90-100/hr
Required Qualifications:
  • Bachelor's degree in Life Sciences, Nursing, Pharmacy, or a related field.
  • Minimum 5 years of Clinical Research Associate (CRA) experience.
  • Direct monitoring experience in kidney transplant and/or kidney transplant clinical studies is required.
  • Strong understanding of ICH-GCP, FDA regulations, and clinical trial processes.
  • Experience managing high-performing academic medical center sites.
  • Excellent organizational, communication, and problem-solving skills.
  • Ability to travel regularly to assigned study sites.
Clinical Resource Network Distinction
CRN, a division of Solomon Page, offers a comprehensive benefits program for hourly employees. We pride ourselves on offering medical, dental, vision, 401(k), telehealth services, ESOP, and commuter benefits to our employees, including consultants - which sets us apart in the industries we serve.
About CRN
Founded in 2002, Clinical Resource Network (CRN), a division of Solomon Page, provides clinical research and talent solutions for pharmaceutical, biotech, and medical device companies. Focused on forming long-term relationships, services encompass contract staffing, project staffing, consultative services, and full-time placements. For more information, visit https://www.solomonpage.com/crn and connect with us on Facebook and LinkedIn .
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