Clinical Research Coordinator jobs in Kansas

Clinical Research Coordinator organizes research information for clinical projects. Selects and observes subjects and assists with data analysis and reporting. Being a Clinical Research Coordinator oversees experiment scheduling and collection of data. Requires a high school diploma or equivalent. Additionally, Clinical Research Coordinator typically reports to a supervisor or manager. The Clinical Research Coordinator works under moderate supervision. Gaining or has attained full proficiency in a specific area of discipline. To be a Clinical Research Coordinator typically requires 1-3 years of related experience. (Copyright 2024 Salary.com)

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Clinical Research Coordinator
  • Innovo Research
  • Hutchinson, KS FULL_TIME
  • Job Summary

    A Research Coordinator is responsible for reviewing, processing, and managing clinical research data and documents, both regulatory and patient records. The CRC performs a variety of clinical procedures, and assists with daily workload planning; ie; collect, record, report, and interpret data on patients enrolled in and/or seeking enrollment in clinical studies according to the protocol, SOPs and GCPs.

    Essential Duties/Responsibilities

    • Provide clinical research support to investigators to prepare for and execute assigned research studies, including:
      • Collect, record, and maintain research subject study data according to study protocols and SOPs, preserving quality control for content, accuracy, and completeness.
      • Collect and submit regulatory/ethics documentation as required by the FDA and other regulatory bodies governing the conduct of clinical research.
      • Recruit and screen participants for clinical trials and maintain subject screening logs.
      • Assist in the initial and ongoing consent process; orient research subjects to the study, including the purpose of the study, procedures, and research process.
      • Maintain source documentation based on protocol requirements.
      • Schedule and execute study visits and perform study procedures.
      • Handle lab testing and analysis, including preparation of specimen collection tubes, shipment, and lab logistics.
      • Monitor subject safety and report adverse events/reactions to the Principal Investigator and/or appropriate medical personnel.
      • Correspond with research subjects and troubleshoot study-related questions or issues.
      • Participate in “huddles” to confirm daily study tasks are assigned to team members and are executed to the expected standards.
    • Assist with study data quality checking and query resolution.
    • Perform a variety of complex clinical research procedures including but not limited to ECG, sample collection, spirometry, vital signs, dose verification, cannulation, and cardiac telemetry monitoring, if needed.
    • Assist investigator in verifying that research study objectives are met on time, within budget and according to applicable protocol requirements, clinical research regulations and quality standards.
    • Provide training to new investigator site staff members on study-specific topics and requirements. Assist in maintaining adherence to investigator site staff training requirements by auditing and maintaining training records.
    • Prepare for and attend study monitoring visits, study audits, and regulatory inspections with clinical research regulatory agencies.
    • Assist research site with coverage planning related to staffing and scheduling for research studies.
    • Performs other duties and projects as assigned.
    Required

    • Bachelor's degree in a related field
    • 1-2 years’ Clinical research experience

    Preferred

    • Relevant work experience in a clinical environment or medical setting, e.g., medical assistant, assistant nurse, laboratory technician; or equivalent combination of education, training, and experience
    • Proficient in the use of Microsoft Office applications
    • Understanding of medical terminology
    • Strong organizational skills

    Skills And Abilities

    • Working knowledge of clinical trials
    • Knowledge and ability to apply GCP/ICH and all applicable FDA regulations and guidelines for human subject protection, drug, and device.
    • In-depth knowledge of departmental, protocol and study-specific operating procedures, consent forms, and study schedules
    • Skilled in carrying out required clinical procedures such as phlebotomy and vital signs.
    • Strong written and verbal communication skills including good command of the English language.
    • Excellent organizational and problem-solving skills.
    • Effective time management skills with the ability to multi-task and manage competing priorities with exceptional attention to details.
    • Ability to establish and maintain effective working relationships with physicians, coworkers, managers, and clients.
    • Practice a high level of integrity, honesty, and in maintaining confidentiality.
  • 2 Days Ago

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Clinical Research Coordinator 182825
  • Medix™
  • Lenexa, KS FULL_TIME
  • Do you love Clinical Research and want your next career step to be someplace with a lot of upward mobility and growth potential? We are looking for a Clinical Research Coordinator to join our growing ...
  • 1 Day Ago

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Clinical Research Assistant/Medical Assistant
  • Alliance for Multispecialty Research
  • Newton, KS FULL_TIME
  • Alliance for Multispecialty Research is a fast-growing clinical research organization that conduct trials for the development of pharmaceuticals. AMR offers competitive pay, 401K matching, health/dent...
  • 22 Days Ago

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RN Clinical Coordinator
  • Clinical Management Consultants
  • Ulysses, KS FULL_TIME
  • A highly accredited hospital near Dodge City, Kansas is looking to bring on an RN Clinical Coordinator to join their team of medical professionals. This hospital has around 120 patient care beds as we...
  • 2 Days Ago

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RN Clinical Coordinator
  • Clinical Management Consultants
  • Dodge, KS FULL_TIME
  • A highly accredited hospital near Dodge City, Kansas is looking to bring on an RN Clinical Coordinator to join their team of medical professionals. This hospital has around 120 patient care beds as we...
  • 2 Months Ago

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Salon Coordinator
  • Sport Clips - Coordinator - KS202
  • Lawrence, KS FULL_TIME
  • Sport Clips is seeking a dynamic and enthusiastic Student Intern to join our team and play a pivotal role in delivering exceptional customer service and ensuring the smooth operation of our salon. If ...
  • 19 Days Ago

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Clinical Research Coordinator
  • Medasource
  • Phoenix, AZ
  • Opening: Clinical Research Coordinator Contract: 6 month Contract to Hire Location: Onsite (Phoenix AZ). Hard Requiremen...
  • 6/2/2024 12:00:00 AM

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Clinical Research Coordinator
  • Medasource
  • Phoenix, AZ
  • Clinical Research Coordinator Start Date: ASAP, flexible Contract: 6 month contract to full-time hire Location: Onsite (...
  • 6/2/2024 12:00:00 AM

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Clinical Research Coordinator
  • Apex Systems
  • Burlingame, CA
  • Apex Systems is seeking a Clinical Research Coordinator to support data collection in the lab. This role will work with ...
  • 6/2/2024 12:00:00 AM

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Clinical Research Coordinator
  • Gastro Health
  • Cincinnati, OH
  • Gastro Health is seeking a Full-Time Clinical Research Coordinator to join our team! Gastro Health is a great place to w...
  • 6/2/2024 12:00:00 AM

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Clinical Research Coordinator
  • Danbury Health Systems
  • Norwalk, CT
  • Clinical Research Coordinator, Norwalk, CT Full-time, 40 hours; 8:30 am - 5:00 pm Nuvance Health has a network of conven...
  • 5/31/2024 12:00:00 AM

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Clinical Research Coordinator
  • CARLE
  • Urbana, IL
  • The Clinical Research Coordinator (CRC) is a specialized research professional that facilitates and coordinates the dail...
  • 5/29/2024 12:00:00 AM

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Assistant Clinical Research Coordinator
  • General Dynamics Information Technology
  • San Diego, CA
  • GDIT's Military Health Team is seeking an Assistant Clinical Research Coordinator in support of the Naval Health Researc...
  • 5/29/2024 12:00:00 AM

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Clinical Research Coordinator
  • Sanford Health
  • Sioux Falls, SD
  • Careers With Purpose Sanford Health is one of the largest and fastest-growing not-for-profit health systems in the Unite...
  • 5/29/2024 12:00:00 AM

Kansas /ˈkænzəs/ (listen) is a U.S. state in the Midwestern United States. Its capital is Topeka and its largest city is Wichita, with its most populated county being Johnson County. Kansas is bordered by Nebraska on the north; Missouri on the east; Oklahoma on the south; and Colorado on the west. Kansas is named after the Kansa Native American tribe, which inhabited the area. The tribe's name (natively kką:ze) is often said to mean "people of the (south) wind" although this was probably not the term's original meaning. For thousands of years, what is now Kansas was home to numerous and divers...
Source: Wikipedia (as of 04/11/2019). Read more from Wikipedia
Income Estimation for Clinical Research Coordinator jobs
$57,324 to $77,293

Clinical Research Coordinator in Rock Hill, SC
A clinical research coordinator coordinates the clinical trials under the guidance of the principal investigator.
October 22, 2019
Clinical Research Coordinator in Binghamton, NY
However, many people start working in research with no experience and can receive on-the-job training and experience.
November 18, 2019
Clinical Research Coordinator in Portsmouth, NH
With an experienced coordinator, just as with an inexperienced one, it’s the same.
December 11, 2019