ZipRecruiter

Log In

1

Clinical Informaticist Jobs in Indiana (NOW HIRING)

previous page

Showing results 21-34

All JobsClinical Informaticist JobsClinical Informaticist Jobs in Indiana

Clinical Informaticist information

See Indiana salary details

$49.5K

$98.6K

$156.1K

How much do clinical informaticist jobs pay per year?

As of Aug 6, 2026, the average yearly pay for clinical informaticist in Indiana is $98,579.00, according to ZipRecruiter salary data. Most workers in this role earn between $71,400.00 and $109,900.00 per year, depending on experience, location, and employer.

What does a clinical informaticist do?

A Clinical Informaticist bridges the gap between clinical practice and information technology within healthcare settings. They work to improve patient care by optimizing the use of electronic health records (EHRs), developing clinical workflows, and ensuring that healthcare data is accurate, accessible, and secure. Clinical Informaticists collaborate with healthcare providers, IT teams, and administrators to implement new technologies and analyze data to support clinical decision-making. Their role is vital in enhancing healthcare quality, efficiency, and patient outcomes.

What are the key skills and qualifications needed to thrive as a clinical informaticist, and why are they important?

To thrive as a Clinical Informaticist, you need a solid background in clinical practice, health informatics, and data analysis, often supported by a degree in healthcare or informatics and relevant certifications like CPHIMS. Familiarity with electronic health record (EHR) systems, clinical decision support tools, and data management platforms is typically required. Strong communication, analytical thinking, and change management skills help bridge the gap between clinical staff and IT teams. These competencies are essential for optimizing healthcare technology, improving patient outcomes, and ensuring effective adoption of digital systems.

What is the best degree for clinical informaticist?

A clinical informaticist typically holds a bachelor's degree in health informatics, nursing, computer science, or a related healthcare or technology field. Many roles also require or prefer a master's degree such as a Master of Health Informatics (MHI) or a Master of Science in Nursing (MSN) with informatics specialization, along with relevant certifications like the Certified Health Data Analyst (CHDA) or Certified Professional in Healthcare Information and Management Systems (CPHIMS).

What is the difference between Clinical Informaticist vs Medical Coder?

AspectClinical InformaticistMedical Coder
CredentialsHealth Informatics certifications, sometimes clinical degreesCertified Coding Specialist (CCS), Certified Professional Coder (CPC)
Work EnvironmentHospitals, clinics, health IT companiesMedical offices, billing companies, hospitals
Industry UsageHealth IT, clinical workflow improvementMedical billing, coding, reimbursement
Search/Comparison IntentUnderstanding roles in health informaticsMedical billing and coding differences

While both Clinical Informaticists and Medical Coders work within healthcare settings, Clinical Informaticists focus on optimizing clinical workflows and health IT systems, often requiring informatics certifications and clinical knowledge. Medical Coders specialize in translating medical documentation into billing codes, primarily needing coding certifications. Their roles differ in scope but are both essential in healthcare operations.

How does a clinical informaticist typically collaborate with healthcare providers and IT teams?

Clinical Informaticists serve as vital liaisons between clinical staff and IT departments, ensuring that electronic health record (EHR) systems and other technologies effectively support patient care. They frequently participate in interdisciplinary meetings, gather feedback from clinicians, and translate clinical needs into technical requirements for system enhancements or troubleshooting. This collaborative approach helps streamline workflows, improve data accuracy, and support compliance with healthcare regulations. Effective communication and the ability to bridge the gap between technical and clinical perspectives are essential for success in this role.
What are popular job titles related to Clinical Informaticist jobs in Indiana? For Clinical Informaticist jobs in Indiana, the most frequently searched job titles are:
What job categories do people searching Clinical Informaticist jobs in Indiana look for? The top searched job categories for Clinical Informaticist jobs in Indiana are:
What are popular job titles related to Clinical Informaticist jobs in IN? For Clinical Informaticist jobs in IN, the most frequently searched job titles are:
Clinical Informaticist jobs near you
Infographic showing various Clinical Informaticist job openings in Indiana as of August 2026, with employment types broken down into 71% Full Time, and 29% Contract. Highlights an 100% In-person job distribution, with an average salary of $98,579 per year, or $47.4 per hour.

Clinical Research Coordinator I -RN

Iterative Health

New Albany, IN • On-site

$63K - $80K/yr

Other

This job post has expired today. Applications are no longer accepted.

Job description

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.

Apply