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Full Time Clinical Research Informatics Jobs (NOW HIRING)

Cook Children's

Research Data Manager

Fort Worth, TX · On-site

... clinical coding systems, and practical experience producing research datasets. Education * Bachelor's degree in Health Information Management, Biomedical Informatics, Public Health, or related field ...

Cook Children's

Research Data Analyst, Senior

Fort Worth, TX · On-site

$111K - $111K/yr

The Sr. Research Data Analyst is a critical member of the Research Informatics team, responsible for enabling compliant researcher access to clinical and research data while protecting patient ...

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Full Time Clinical Research Informatics information

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$52K

$103.6K

$164K

How much do full time clinical research informatics jobs pay per year?

As of Sep 3, 2026, the average yearly pay for full time clinical research informatics in the United States is $103,597.00, according to ZipRecruiter salary data. Most workers in this role earn between $75,000.00 and $115,500.00 per year, depending on experience, location, and employer.

What is the difference between Full Time Clinical Research Informatics vs Clinical Data Analyst?

AspectFull Time Clinical Research InformaticsClinical Data Analyst
CredentialsTypically requires a degree in health informatics, computer science, or related field; certifications like CPHIMS are commonUsually holds a degree in health informatics, statistics, or related field; certifications are less common
Work EnvironmentWorks in clinical research settings, hospitals, or research organizations, focusing on data systems and EHR integrationWorks primarily with data analysis, reporting, and data management in healthcare or research settings
Employer & Industry UsageUsed by research institutions, pharmaceutical companies, and healthcare providers involved in clinical trialsEmployed across healthcare, research, and pharmaceutical industries for data management and analysis

Full Time Clinical Research Informatics focuses on managing and integrating clinical research data systems, requiring informatics expertise. Clinical Data Analysts primarily analyze and interpret data, often with less emphasis on informatics systems. Both roles overlap in data handling but differ in scope and technical focus.

What cities are hiring for Full Time Clinical Research Informatics jobs?

Cities with the most Full Time Clinical Research Informatics job openings:

What are the most commonly searched types of Clinical Research Informatics jobs?

The most popular types of Clinical Research Informatics jobs are:

What states have the most Full Time Clinical Research Informatics jobs?

States with the most job openings for Full Time Clinical Research Informatics jobs include:

Full Time Clinical Research Informatics jobs near you

Clinical Research Coordinator

Rocky Mountain Clinical Research

Idaho Falls, ID • On-site

$17 - $25/hr

Full-time

Medical, Dental, Vision, Retirement, PTO

Re-posted yesterday

Job description

Clinical Research Coordinator (Full-Time)
Rocky Mountain Clinical Research Idaho Falls, ID
Rocky Mountain Clinical Research is seeking a full-time Clinical Research Coordinator (CRC) to join our growing team in Idaho Falls, ID. This is an excellent opportunity for a healthcare professional looking to expand into clinical research while making a meaningful impact on patient care and the future of medicine.
If you enjoy working directly with patients, value precision and organization, and want to be part of a collaborative, mission-driven research organization, we encourage you to apply.
Compensation & Benefits
  • Hourly wage: $17 - $25 per hour (based on education, training, and experience)
  • Benefits package includes:
    • Medical, dental, and vision insurance
    • 401(k) retirement plan
    • Paid time off (PTO)
  • Full-time, stable position with opportunities for professional growth

About Rocky Mountain Clinical Research
Rocky Mountain Clinical Research was founded on the principle of advancing medical care for patients facing complex diseases. We conduct high-quality clinical research across a range of therapeutic areas, including diabetes, evaluating medications and medical devices to determine their safety and effectiveness compared to current standards of care.
As an investigator-led, patient-focused research site, we play a key role in bringing new treatments to market while ensuring patient safety and regulatory compliance. We are a family-oriented organization that values teamwork, integrity, and long-term employee success.
Position Summary: Clinical Research Coordinator
The Clinical Research Coordinator plays a critical role in the day-to-day execution of clinical trials. Working closely with the Principal Investigator, Research Director, and study team, the CRC ensures that clinical studies are conducted in compliance with study protocols, Good Clinical Practice (GCP), and federal regulations.
This role combines patient interaction, clinical coordination, and administrative responsibilities, making it ideal for detail-oriented healthcare professionals who enjoy both people-facing and organizational work.
Key Responsibilities
  • Coordinate and administer clinical trials under the direction of the Principal Investigator
  • Screen, enroll, consent, and follow study participants
  • Ensure participant safety and protocol adherence throughout the study lifecycle
  • Maintain accurate source documentation and regulatory files
  • Complete study-related data entry and follow-up documentation with high attention to detail
  • Prepare for and support sponsor, monitor, and regulatory audits
  • Collaborate with investigators, sponsors, monitors, and internal research staff
  • Ensure studies are conducted in compliance with GCP, FDA regulations, and study protocols

Required Qualifications
  • Healthcare or medical background (clinical or patient-facing experience)
  • Strong clerical, organizational, and documentation skills
  • Excellent interpersonal and communication skills
  • High attention to detail and commitment to quality and accuracy
  • Ability to work independently while collaborating effectively with a team

Preferred Qualifications
  • Certified Medical Assistant (CMA), Licensed Practical Nurse (LPN), Registered Nurse (RN), or higher credentialing
  • Experience in a healthcare, research, or clinical trial environment
  • Familiarity with Good Clinical Practice (GCP), clinical trial protocols, or regulatory documentation
  • Strong analytical and decision-making skills

Clinical research experience is preferred but not required- GCP and CRC training will be provided for motivated candidates.
Work Schedule
  • Full-time
  • Monday - Friday
  • Occasional (but rare) weekends or major holidays required

Ready to Join Our Team?
If you're passionate about patient care, clinical excellence, and contributing to the future of medicine, we'd love to hear from you. Join our team of 25 Clinical Research Coordinators where your work truly makes a difference.
Apply today to become part of Rocky Mountain Clinical Research.
We understand your time is valuable, so we have a very quick and easy application process. If you feel that you have the right medical or nursing background for this clinical study job, please fill out our initial 3-minute, mobile-friendly application. We look forward to meeting you!
Location: 83404

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