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Clinical Trial Risk Based Monitoring Jobs in Kentucky

Solomon Page

Contract CRA

Covington, KY · On-site

$90 - $100/hr

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 ...

Solomon Page

Contract CRA

Covington, KY · On-site

$90 - $100/hr

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 ...

Berger Health System

$150 - $210/hr

Clinical trial budget development and negotiation Clinical trial contract negotiation and ... Operational risk assessment and mitigation**Business Leadership*** Strategic planning*

Abbott Laboratories

$99 - $199/hr

... monitoring, and study closeout activities.* Collaborate with investigators and site personnel to ... Effectively communicate clinical data, trial objectives, and evidence-based recommendations to ...

Syneos Health, Inc.

$80 - $140/hr

Draft and finalize clinical trial agreements that balance business objectives with legal and ... risk during the contract life cycle. * Participates in creating and delivering solutions for ...

WEP Clinical Inc.

$140 - $180/hr

... drive effective, risk-based decisions and operational improvements. The Senior GMDP Quality ... Through end‑to‑end clinical trial delivery, home health services, expanded access programs, and ...

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Xencor

$195 - $240/hr

... trial process and data management, clinical operations, biometrics, quality management, and systems applications to support operations * Competency in multiple computer-based tools, in addition to ...

Amgen SA

$180 - $240/hr

Our award-winning culture is collaborative, innovative, and science based. If you have a passion ... Support review, analysis, and presentation preparation of clinical trial data for internal decision ...

Empower LLC

$152 - $220/hr

Demonstrated success designing scalable compliance controls and risk-based monitoring programs* Continuous improvement mindset with a track record of strengthening compliance processes and controls*

Janux Therapeutics, Inc.

$170 - $182/hr

... of clinical trial-related agreements and serve as the key liaison between Clinical Operations ... based on factors such as qualifications, skill level, competencies, internal equity, and work ...

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Clinical Trial Risk Based Monitoring information

What is clinical trial risk based monitoring?

Clinical Trial Risk Based Monitoring (RBM) is a strategy used in clinical research to prioritize and focus monitoring activities on the most critical risks to patient safety and data integrity. Instead of monitoring every data point equally, RBM uses data analytics and risk assessment tools to identify which sites, processes, or data require more attention. This approach increases efficiency, reduces costs, and helps ensure that potential issues are detected and addressed promptly. RBM is supported by regulatory agencies and is increasingly adopted in both large and small clinical trials.

How does a clinical trial risk based monitoring professional typically collaborate with cross-functional teams during a study?

In a Clinical Trial Risk Based Monitoring role, you will regularly work with clinical research associates, data managers, statisticians, and regulatory teams to identify and address potential risks throughout a study. Collaboration often involves participating in meetings to review data trends, sharing insights about site performance, and helping to develop mitigation strategies. Effective communication is crucial, as you will be responsible for ensuring that all stakeholders are informed of key risks and recommended actions. This collaborative environment helps drive patient safety, data integrity, and overall trial success.

What are the key skills and qualifications needed to thrive in clinical trial risk based monitoring, and why are they important?

To thrive in Clinical Trial Risk Based Monitoring, you need expertise in clinical research, regulatory compliance, and data analysis, usually supported by a degree in life sciences or related fields. Familiarity with risk assessment tools, EDC (Electronic Data Capture) systems, and GCP (Good Clinical Practice) certification is typically required. Strong attention to detail, critical thinking, and effective communication help professionals proactively identify and address potential risks in trials. These skills are crucial for maintaining data integrity, ensuring patient safety, and optimizing the efficiency and quality of clinical studies.

What is the difference between Clinical Trial Risk Based Monitoring vs Clinical Trial Data Manager?

AspectClinical Trial Risk Based MonitoringClinical Trial Data Manager
Primary FocusMonitoring trial sites for risks and complianceManaging and ensuring accuracy of trial data
Required SkillsMonitoring protocols, regulatory knowledge, site managementData management, database systems, quality control
Work EnvironmentClinical sites, monitoring visits, remote oversightData centers, clinical trial databases, office setting
CertificationsGCP, monitoring certificationsCDMP, data management certifications

While both roles are integral to clinical trials, Risk Based Monitoring focuses on overseeing site performance and compliance to mitigate risks, whereas Data Managers concentrate on managing and validating trial data for accuracy and integrity.

What are popular job titles related to Clinical Trial Risk Based Monitoring jobs in Kentucky?

For Clinical Trial Risk Based Monitoring jobs in Kentucky, the most frequently searched job titles are:

What job categories do people searching Clinical Trial Risk Based Monitoring jobs in Kentucky look for?

The top searched job categories for Clinical Trial Risk Based Monitoring jobs in Kentucky are:

What cities in Kentucky are hiring for Clinical Trial Risk Based Monitoring jobs?

Cities in Kentucky with the most Clinical Trial Risk Based Monitoring job openings:

Clinical Trial Risk Based Monitoring jobs near you
Infographic showing various Clinical Trial Risk Based Monitoring job openings in Kentucky as of August 2026, with employment types broken down into 1% As Needed, 76% Full Time, 15% Part Time, 7% Contract, and 1% Nights. Highlights an 87% Physical, 3% Hybrid, and 10% Remote job distribution.

Contract CRA

Solomon Page

Covington, KY • On-site

$90 - $100/hr

Contractor

Medical, Dental, Vision, Retirement

Re-posted 29 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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