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Manager Clinical Research Informatics Jobs in Kentucky

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Feasibility Informatics Manager

Lexington, KY · On-site

  • Medical

  • Dental

  • Vision

  • Life

  • Retirement

Feasibility Informatics Manager ICON is a global healthcare intelligence and clinical research organisation united by a mission to bring new medicines and treatments to patients faster. As a values ...

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Senior Clinical Research Associate

Lexington, KY · Remote

  • Medical

  • Dental

  • Vision

  • Life

  • Retirement

... clinical research organisation united by a mission to bring new medicines and treatments to ... As a Senior CRA at ICON Plc, you will oversee and manage clinical trial activities to ensure they ...

Ora

Clinical Research Coordinator I

Louisville, KY · On-site

$23.25 - $31/hr

  • Medical

  • Dental

  • Vision

  • Life

Our CRC I's will partner with tenured Clinical Research Coordinators and Clinical Project Managers to execute protocol directives and work cross-functionally with internal and external teams such as ...

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Infographic showing various Manager Clinical Research Informatics job openings in Kentucky as of August 2026, with employment types broken down into 88% Full Time, 11% Part Time, and 1% Contract. Highlights an 84% Physical, 3% Hybrid, and 13% Remote job distribution.

Clinical Research Nurse Practitioner

Monroe Biomedical Research

Louisville, KY • On-site

Full-time

Medical, Dental, Vision

Posted 8 days ago

Job description

MBR - Louisville, KY | Onsite
ABOUT THE ROLE
Monroe Biomedical Research is growing, and we are seeking an experienced, patient-focused Clinical Research Nurse Practitioner to join our Louisville team.
This unique role combines advanced clinical practice with hands-on clinical research coordination. The Clinical Research Nurse Practitioner will work directly with study participants while supporting the successful execution of clinical trials from patient screening and study visits through documentation and follow-up.
This is an excellent opportunity for an NP who enjoys direct patient care, thrives in a fast-paced clinical environment, and is interested in contributing to research that advances medicine and expands treatment options for patients.
WHAT YOU'LL DO
Clinical Research & Study Management
• Coordinate and manage clinical trial visits from screening through study completion
• Review study protocols and ensure required procedures and assessments are completed accurately and within protocol-defined timelines
• Develop and maintain accurate and complete source documentation in accordance with study protocols
• Support participant screening, enrollment, and ongoing study activities
• Work closely with investigators, sponsors, monitors, and internal research staff to support successful study execution
• Ensure clinical trials are conducted in accordance with Good Clinical Practice (GCP), FDA regulations, sponsor requirements, and internal procedures.
Patient Care & Clinical Responsibilities
• Provide clinical assessment and care to adult study participants within the scope of NP practice and study protocol requirements
• Perform and/or oversee study-related clinical procedures, including blood draws, ECGs, pulmonary function testing, vital signs, and other protocol-required assessments
• Review relevant medical history, medications, laboratory results, and other clinical information
• Educate participants regarding study requirements, procedures, medications, and follow-up expectations
• Identify and communicate changes in participant condition, adverse events, or other clinically significant findings to appropriate study team members
• Provide a professional, compassionate, and supportive experience throughout each participant's clinical trial journey.
Data, Documentation & Quality
• Review and process medical records and study-related clinical documentation
• Accurately document study visits and clinical findings
• Enter and maintain study data in sponsor and clinical research systems accurately and within required timelines
• Prepare, process, and coordinate shipment of laboratory specimens according to protocol requirements
• Respond to data queries and assist with maintaining complete, inspection-ready study records
QUALIFICATIONS
• Current Nurse Practitioner (NP) licensure with the ability to practice with an adult patient population
• Master's degree in Nursing or related advanced practice field required
• Previous experience providing direct patient care required
• Clinical research experience strongly preferred
• Strong clinical judgment and commitment to patient safety
• Excellent attention to detail, organization, and documentation skills
• Ability to interpret and follow detailed clinical trial protocols
• Ability to effectively manage competing priorities and multiple studies in a fast-paced research environment
• Strong communication and interpersonal skills with a patient-centered approach
WHY JOIN MONROE BIOMEDICAL RESEARCH?
• Join a growing clinical research organization contributing to the advancement of new treatments and therapies
• Work alongside a collaborative and supportive multidisciplinary research team
• Gain exposure to a diverse portfolio of clinical trials
• Opportunity to combine advanced clinical skills with clinical research experience
• 100% company-paid employee Health, Dental, and Vision insurance

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