Top 52 Clinical data coordinator Jobs in Louisville, Ky

Clinical Research Coordinator I -RN
Iterative Health —New Albany, IN
- Nursing
- RN License
- Quality control
Quick Apply
Clinical Research Coordinator II - New Albany, IN
Iterative Health —New Albany, IN
- Full-time
- Mid-level
- 3 years
- Bachelor's degree
Quick Apply
Clinical Supervisor (BCBA)
Center for Autism and Related Disorders —Louisville, KY
- $73,000 - $113,000 a year
- Full-time
- Microsoft Outlook
- Current TB test
- HIPAA
- Paid training
- Relocation assistance
Quick Apply
Appointment Coordinator
FIRST UROLOGY P S C —Louisville, KY
- Full-time
- Background check
- Microsoft Excel
- Microsoft Outlook
- AD&D insurance
- Paid holidays
Quick Apply
Patient Access and Intake Coordinator Full Time
Kindred Hospitals Dallas/Ft Worth District —Louisville, KY
- Full-time
- Hospital
- English
- Mid-level
6d
Clinical Research Coordinator I
Ora —Louisville, KY
- Weekends as needed
- Vital signs
- Clinic experience
- Clinic
- Dental insurance
Quick Apply
Clinical Research Coordinator assitant
Quantum Research Associates —Louisville, KY
- $16 - $18 an hour
- Full-time
- Microsoft Excel
- Microsoft Outlook
- Computer literacy
Quick Apply
1d
Clinical Research Coordinator II
Iterative Health —New Albany, IN
- Patient monitoring
- HIPAA
- Mid-level
Credentialing Specialist
Trusted Medical PLLC —Louisville, KY
- $52,123 - $57,456 a year
- Full-time
- System design
- Research
- Mid-level
Quick Apply
14d
Central Eligibility Authorization Team Coordinator
BrightSpring Health Services —Louisville, KY
- Full-time
- Mid-level
- High school diploma or GED
- Continuous improvement
AR Coordinator-Clinical
Trilogy Health Services —Louisville, KY
- Full-time
- Research
- Mid-level
- High school diploma or GED
- Health savings account
- Loan repayment program
Clinical Research Coordinator V
University of Louisville —Louisville, KY
- $48,225 - $72,389 a year
- Online Application
- Mid-level
- Bachelor's degree
- Team management
9d
Admission Coordinator
Bristol Hospice, LLC —New Albany, IN
- $20 - $25 an hour
- Full-time
- 18 years or older
- Mid-level
- Office
- Mileage reimbursement
- Health savings account
Quick Apply
Patient Care Coordinator
Associates in Dermatology —Louisville, KY
- $18 - $20 an hour
- Full-time
- English
- High school diploma or GED
- Typing
Quick Apply
Front Desk Coordinator
Ellis and Badenhausen Ortho —Louisville, KY
- US work authorization
- Communication skills
- Entry level
- Profit sharing
- 401(k)
Quick Apply
Administrative Assistant
FIRST UROLOGY P S C —Jeffersonville, IN
- Weekends as needed
- Background check
- Google Workspace
- Microsoft Outlook
- AD&D insurance
- Paid holidays
Quick Apply
Front Desk / Call Center Receptionist
Associates in Dermatology —Louisville, KY
- English
- High school diploma or GED
- Typing
Credentialing Coordinator, Jewish Hospital, Medical Staff Office, 8a-5p
UofL Health —Louisville, KY
- Full-time
- Hospital
- Medical office experience
- Mid-level
Medical Assistant / Dermatology Tech
Associates in Dermatology —Louisville, KY
- Nursing
- Anatomy knowledge
- Vital signs
Clinical Lab Scientist
US Veterans Health Administration —Louisville, KY
- $89,466 - $116,312 a year
- Online Application
- Background check
- OSHA
- Pass drug screening
- Paid parental leave
- Paid holidays
5d

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Clinical Research Coordinator I -RN

Iterative Health -
New Albany, IN

Quick Apply

Job Details

Qualifications

RN License

Full Job Description

Iterative Health is a healthcare technology and services company powering the acceleration of clinical research to transform patient outcomes.

We built a leading performance-driven network of 100+ sites across the US, Europe, India, and Australia, conducting research directly in the communities where care is delivered across gastrointestinal, hepatology, obesity, and cardiology. By combining deep clinical trial expertise with cutting-edge AI, we connect sponsors' scientific ambitions with high-performing research teams that expedite and expand access to novel therapeutics for patients in need. Today, Iterative Health is headquartered in Cambridge, Massachusetts, and New York City with 250+ employees world-wide.

A Clinical Research Coordinator I – RN at Iterative Health is an essential member of the site research team, supporting, facilitating, and coordinating the daily execution of clinical trials across our network. This role is at the heart of every study — managing patient interactions, ensuring protocol compliance, maintaining data integrity, and keeping the operational machinery of clinical research running smoothly.

The ideal candidate brings clinical research experience, a patient-first mindset, strong attention to detail, and the ability to thrive in a fast-paced, protocol-driven environment. This role provides a strong foundation for success while offering a clear path for professional growth within Iterative Health's expanding site network.

Where You'll Drive Impact

Administratively and clinically manage industry-sponsored clinical trials, including problem-solving, communication, and protocol management.
Schedule all patient research visits and procedures in accordance with protocol requirements.
Ensure relevant study and subject-specific information is entered into the CTMS on a regular basis.
Complete and maintain study documentation including consent forms, source documentation, progress notes, case report forms, and investigational accountability forms.
Complete and maintain case report forms per FDA guidelines, reviewing them against patient medical records for completeness and accuracy.
Schedule and prepare for monitor visits.
Maintain inventory of study equipment and supplies onsite at all times.

Lead patient recruitment activities including chart reviews, protocol discussions with patients, and verification of informed consent documentation.
Conduct patient visits as outlined within each study protocol.
Act as the primary point of contact for study participants throughout the course of the study.

Dispense study medication, collect vital signs, and perform ECGs per protocol.
Perform blood draws; process and ship specimens per study protocol and IATA regulations.
As assigned: place IVs, administer IV medications and fluids, give intramuscular and subcutaneous injections, monitor patients during infusion, and discharge patients in accordance with protocol and site policies.

Adhere to Research SOPs, Good Clinical Practice (GCP) guidelines, and study protocols at all times.
Assist with routine data verification and quality control, ensuring data integrity and consistency with prescribed study protocols.
Ensure all safety data is reviewed by the PI in a timely manner.
Cooperate with site compliance and monitoring efforts regarding the access, use, and disclosure of PHI; report instances of noncompliance to the appropriate compliance office.
Assist the study team in protecting the rights and welfare of all human research participants in accordance with federal regulations.
Maintain ongoing communication with the CRO, sponsor, research participants, Site Manager, and PI throughout the course of each study.
Actively participate in communication of status and results to management.

Perform job related duties as requested

What You Bring to the Team

Active Registered Nurse (RN) license required.
1–2 years of clinical research experience strongly preferred .
Solid nursing background with a concentration in, or willingness to develop advanced knowledge of, GI specialty.
Ability to execute research tasks with guidance from experienced staff, PIs, and management.
Strong written and verbal communication skills.
Ability to read, interpret, and apply clinic policies and research protocols.
Proficiency in standard office software and CTMS platforms.
Highly organized with the ability to manage multiple priorities and meet deadlines.
Ability to work independently and collaboratively in a fast-paced environment.

Preferred Qualifications

Prior GI or hepatology clinical research experience.
Familiarity with GCP guidelines and FDA regulations governing clinical research.
Experience with CTMS, EDC, or eTMF platforms.
ACRP or SOCRA certification (CCRC or CCRP), or active pursuit of certification.

At Iterative Health, we're actively working towards creating an environment that is representative of the diversity of patients our technology serves. We are focused on building an equitable and inclusive culture, and by extension, hiring process. If you require any accommodations to make the application process or interviewing experience more accessible to you, please contact [email protected].

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Refine Your Search

clinical data coordinator jobs in louisville, ky

Clinical Research Coordinator I -RN

Clinical Research Coordinator II - New Albany, IN

Clinical Supervisor (BCBA)

Appointment Coordinator

Patient Access and Intake Coordinator Full Time

Clinical Research Coordinator I

Clinical Research Coordinator assitant

Clinical Research Coordinator II

Credentialing Specialist

Central Eligibility Authorization Team Coordinator

AR Coordinator-Clinical

Clinical Research Coordinator V

Admission Coordinator

Patient Care Coordinator

Front Desk Coordinator

Administrative Assistant

Front Desk / Call Center Receptionist

Credentialing Coordinator, Jewish Hospital, Medical Staff Office, 8a-5p

Medical Assistant / Dermatology Tech

Clinical Lab Scientist

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