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Research Study Jobs in Kentucky (NOW HIRING)

Washington University

$75 - $129/hr

Responsible for overall clinical research study planning, coordinating, and execution of all study-related activities, including extensive interaction wth the Internal Review Board (IRB), study ...

usf.edu

$90 - $120/hr

Responsible for management of the screening, enrollment, and retention of study participants, ensuring quality of data collected throughout the research study, assisting/training staff and ...

New

Actox

$80 - $100/hr

The successful candidate will serve as Project Lead in cell-based and animal use research studies on environmental and occupational exposures to identify health effects before health and operational ...

New

Washington University

$63 - $115/hr

Assists in the planning, design, implementation, and coordination of multidisciplinary research studies and laboratory operations that range from molecular imaging, cancer biology, antibody ...

Manhattan Strategy Group

$150 - $210/hr

Ensure that applied research studies, tools, research products, and dissemination materials meet standards for rigor, relevance, quality, clarity, plain language, and accessibility. * Oversee ...

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Research Study information

What is a research study?

A Research Study job involves conducting investigations to gather, analyze, and interpret data on a specific topic. Professionals in this role design experiments, collect information from various sources, and summarize findings to contribute to scientific or academic knowledge. They may work in universities, healthcare, corporate research, or government agencies. Responsibilities can include literature reviews, data collection, statistical analysis, and report writing.

What are the typical daily responsibilities of someone working in a research study role?

Daily responsibilities in a Research Study role often include collecting and managing data, recruiting and coordinating with study participants, and maintaining accurate documentation of research activities. You may also be involved in designing study protocols alongside lead researchers, analyzing results using statistical software, and preparing progress reports or manuscripts for publication. Collaboration is common, as you'll work closely with principal investigators, research assistants, and sometimes external partners. Attention to detail and strict adherence to ethical standards are important in ensuring reliable and valid study outcomes.

What are the key skills and qualifications needed to thrive in the research study position?

To succeed in a Research Study position, you typically need strong analytical skills, attention to detail, and a background in scientific or social science research methodology—usually supported by a relevant degree. Familiarity with data analysis software like SPSS, R, or Python, as well as experience with survey tools and ethics certifications (such as CITI training), is frequently required. Excellent written and verbal communication, organization, and collaboration skills set top candidates apart. These competencies are crucial for accurately collecting, analyzing, and presenting data while working effectively within multidisciplinary research teams.

What kind of careers are in research study?

Careers in research study include roles such as research coordinators, data analysts, research assistants, and principal investigators. These positions often require skills in data collection, analysis, and reporting, and may involve working in clinical, academic, or industry settings with adherence to ethical standards and regulatory guidelines.

What are popular job titles related to Research Study jobs in Kentucky?

For Research Study jobs in Kentucky, the most frequently searched job titles are:

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

The top searched job categories for Research Study jobs in Kentucky are:

Research Study jobs near you
Infographic showing various Research Study job openings in Kentucky as of August 2026, with employment types broken down into 1% As Needed, 83% Full Time, 8% Part Time, 7% Temporary, and 1% Contract. Highlights an 78% Physical, 4% Hybrid, and 18% Remote job distribution.

Clinical Research Nurse Practitioner

Louisville, KY • On-site

Monroe Biomedical Research
Pharmaceutical and Medicine Manufacturing • 11 - 50 employees
Learn more about Monroe Biomedical Researchexternal

Full-time

Medical, Dental, Vision

Posted 18 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

Apply