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Full Time Clinical Research Informatics Jobs in Missouri

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... Informatics (DBEI) and the Antimicrobial Resistance, Healthcare Epidemiology and Antimicrobial Stewardship (ARES) Research Collaborative at the University of Pennsylvania seeks a full-time Clinical ...

  • Medical

  • Dental

  • Vision

  • Life

  • Retirement

... Informatics (DBEI) and the Antimicrobial Resistance, Healthcare Epidemiology and Antimicrobial Stewardship (ARES) Research Collaborative at the University of Pennsylvania seeks a full-time Clinical ...

$54K - $81K/yr

  • Medical

  • Retirement

  • PTO

... clinical research program ... This full-time position plays an essential role in advancing our understanding of cerebrovascular ...

$22.50 - $30/hr

  • Medical

  • Retirement

  • PTO

Collects clinical data under clinical research protocols. * Performs other duties as assigned ... The Transplant Nephrology Section is looking for a third full time research coordinator (level 1 or ...

$22.50 - $30/hr

  • Medical

  • Retirement

  • PTO

Collects clinical data under clinical research protocols. * Performs other duties as assigned ... The Transplant Nephrology Section is looking for a third full time research coordinator (level 1 or ...

$25.14 - $35.24/hr

Regular Time Type: Full time Scheduled Weekly Hours: 40 Department: 400178 Cancer Center/Clin ... The Clinical Research Regulatory Support Specialist II independently administers the Wilmot Cancer ...

Showing results 21-40

Full Time Clinical Research Informatics information

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

The most popular types of Clinical Research Informatics jobs in Missouri are:

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

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

Clinical Research Coordinator - Women's Health Department

Truman Medical Centers

Kansas City, MO • On-site

$23.75 - $31.50/hr

Full-time

Re-posted 18 days ago


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Clinical Research Coordinator - Women's Health Department101 Truman Medical CenterJob LocationUniversity Health Truman Medical CenterKansas City, Missouri
Department
Admin Womens Health UHTMC
Position Type
Full time
Work Schedule
8:00AM - 4:30PM
Hours Per Week
40
Job Description
Responsible for performing diverse administrative and clinical responsibilities requiring some analysis, sound judgment, and a high level of knowledge of specific research study protocols, Good Clinical Practice Guidelines, Federal research regulations, and institutional requirements. Responsible for coordination and management of clinical study protocols and along with the research investigator, manages many aspects of the clinical trial and conducts all research activities within an ethically based framework in accordance with federal, state, and local regulations. Function as a liaison between investigators, subjects and sponsors, the Institution(s), Institutional Review Board (IRB) and Privacy Board.

Minimum Requirements

  • Bachelor's degree in allied health medical field, another related field or licensed LPN.

  • Ability to prioritize and complete several tasks/projects simultaneously in strict accordance with regulations, policies, and study protocol.

  • Demonstrated effective verbal/written communication skills, analytical skills, attention to details, and ability to work independently with minimal supervision.

  • Organization/time management skills and project management skills.

  • Demonstrated intermediate knowledge of personal computer skills.

Preferred Qualifications

  • One year clinical research experience.

  • Clinical Research Coordinator Certification (by either the Association for Clinical Research Professionals or Society of Clinical Research Associates).

  • Knowledge of Good Clinical Practices, U.S. Department of Health and Human Services Protection of Human Subjects and U.S. Food and Drug Administration regulations, International Conference of Harmonization Guidelines, and the HIPAA Privacy Rule as it impacts clinical research


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