Clinical Research Coordinator jobs in the United States

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/HC Research Associate - ICTS Research Coordinator Core
  • ICTS Research Coordinator Core - Jobs@UIOWA Careers
  • Iowa, IA FULL_TIME
  • The University of Iowa Institute for Clinical and Translational Science (ICTS) Research Coordinator Core is seeking a clinical / health care research associate to be an integral member of the research team. This position will provide support for the ICTS by performing activities which are vitally important to ICTS mission, as well as to grow and foster innovation through research support endeavors. The clinical / health care research associate will design, plan, promote, and control clinical research trials and coordinate the processing and analysis of trials data as well as assist with the development and maintenance of regulatory, data and budget documents. 

    Duties to include but not limited to:

    ·         Screen patient for study eligibility and consent for clinical trials.

    ·         Educate patient on scope of study, potential risks and benefits, possible alternatives, and study requirements.

    ·         Assist in the design, development, execution, administration, and maintenance of protocols and clinical studies.

    ·         Provide input into descriptions of complex research procedures.

    ·         Screen, recruit, enroll, and obtain informed consent for clinical research activities.

    ·         Oversee recruitment of subjects and scheduling of trial-related procedures.

    ·         Participate in the collection, and entry of data into clinical research trial data systems.

    ·         Manage and organize regulatory documents.

    ·         Prepare regulatory submissions. 

    For a full job description, please send an e-mail to the contact listed below. 

    About ICTS: The Institute for Clinical and Translational Science (ICTS) at the University of Iowa was approved by the Iowa Board of Regents in 2007 to support the work of investigators involved in clinical and translational science. Our mission is to accelerate translational science through programs to develop the translational workforce, to promote engagement of community members and other stakeholders, to promote research integration across the lifespan, and to catalyze innovative clinical and translational research. These efforts will lead to the development of novel therapies and healthcare delivery strategies, the integration of translational research and clinical practice, and, ultimately to measurable improvements in the health of Iowa and the nation. 

    Percent of Time: 100%

    Pay Grade: 5A

    https://hr.uiowa.edu/pay/guide-pay-plans

     Benefits Highlights:

    Regular salaried position located in Iowa City, Iowa

    Fringe benefit package including paid vacation; sick leave; health, dental, life and disability insurance options; and generous employer contributions into retirement plans

    For more information about Why Iowa?, click here

    Required Qualifications

    ·         Bachelor’s degree in Nursing (BSN) or an equivalent combination of education and experience is required.

    ·         Minimum of 2 years clinical nursing experience or 1 year of clinical research experience is required.

    ·         Excellent written and verbal communication skills with patients/families, and interdisciplinary team members as demonstrated through written and verbal interactions are required.

    ·         Working knowledge of Good Clinical Practice (GCP). 

    ·         Ability to work flexible hours including nights, evenings, and weekends as needed by the research protocol is required.

    ·         A current license to practice nursing in the state of Iowa by the time of hire is required.

    ·         General computer skills are required. 

    Desirable Qualifications

    ·         Strong Clinical Practice skills with work in a clinical practice area within the past year.

    ·         Experience with cell therapy and/or chemotherapy infusions.

    ·         Certification in ACLS, NRP or PALS.

    ·         Experience in processing research regulatory documents and budget preparation is desirable.

    ·         Experience developing education and orientation materials is desired.

    ·         The ability to adapt to frequently changing duties and work environment is desired.

    ·         The ability to work independently is desired.

    ·         Excellent time management skills and ability to perform detail-oriented work is desired. 

    Application Process:

    In order to be considered for an interview, applicants must upload the following documents and mark them as a “Relevant File” to the submission:

    Resume

    Cover Letter 

    Job openings are posted for a minimum of 14 calendar days and may be removed from positing and filled any time after the original posting period has ended. 

    Successful candidates will be required to self -disclose any conviction history and will be subject to a criminal background check and credential/education verification. Up to 5 professional references will be requested at a later step in the recruitment process.

    On Campus: This position is performed fully on campus.

     

    Hybrid within Iowa: This position is eligible for a combination of on-campus and remote work. Remote work must be performed at a location within the state of Iowa and comply with the remote work program and related policies.

     

    Remote within Iowa: This position is eligible for primarily remote work but may require limited work onsite at times. Remote work must be performed at a location within the state of Iowa and comply with the remote work program and related policies.

    For additional questions, please contact Dori Hinson at dori-hinson@uiowa.edu. 

    This position is not eligible for University sponsorship for employment authorization.

    Additional Information
    Compensation
    Contact Information
  • 6 Days Ago

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Clinical Research Coordinator I
  • DM Clinical Research
  • Boston, MA FULL_TIME
  • Lab TechnicianThe Lab Technician will be responsible for assisting the clinical research staff in conducting clinical research trials.Duties & Responsibilities:Prepares, processes, and ships laborator...
  • 11 Days Ago

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Clinical Research Coordinator III
  • DM Clinical Research
  • Dallas, TX FULL_TIME
  • Clinical Research Coordinator IIIA CRC III will ensure that quality research is conducted at assigned investigative sites in accordance with the sponsor protocol, FDA Regulations, and ICH/GCP guidelin...
  • 14 Days Ago

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Clinical Research Coordinator (Experienced)
  • Irvine Clinical Research
  • Irvine, CA FULL_TIME
  • Irvine Clinical Research, a research site specializing in late phase CNS clinical trials, is seeking applicants for a Clinical Research Coordinator with previous clinical trial experience. The CRC wil...
  • 16 Days Ago

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Clinical Research Coordinator
  • Ideal Clinical Research Inc
  • Miami, FL FULL_TIME
  • Company Description Ideal Clinical Research Inc is a clinical research organization located in Miami, FL. We take great pride in serving our sponsors with more than 4 South Florida locations. We condu...
  • Just Posted

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Clinical Research Coordinator I
  • Irvine Clinical Research
  • Irvine, CA FULL_TIME
  • Irvine Clinical Research, a research site specializing in clinical trials of Alzheimer's Disease, is seeking applicants for a Clinical Research Coordinator I. The CRC will work under close supervision...
  • 3 Days Ago

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Clinical Research Coordinator
  • Amerit Consulting
  • Los Angeles, CA
  • Overview: Our client, a Medical Center facility under the aegis of a California Public Ivy university and one of largest...
  • 5/19/2024 12:00:00 AM

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Assistant Clinical Research Coordinator
  • UCLA Health
  • Los Angeles, CA
  • General Information Press space or enter keys to toggle section visibility Work Location: Los Angeles, USA Onsite or Rem...
  • 5/19/2024 12:00:00 AM

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Clinical Research Coordinator
  • Amerit Consulting
  • Los Angeles, CA
  • Our client, a Medical Center facility under the aegis of a California Public Ivy university and one of largest health de...
  • 5/17/2024 12:00:00 AM

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Clinical Research Coordinator
  • Headlands Research
  • Palos Verdes Peninsula, CA
  • Overview Headlands Research and Peninsula Research Associates are working together to build the best clinical trial comp...
  • 5/17/2024 12:00:00 AM

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Clinical Research Coordinator
  • Talent Healthcare Staffing Services
  • Los Angeles, CA
  • Location: 11800 Wilshire Blvd. Los Angeles Float Location: 1919 Santa Monica Blvd. Required: BCLS certified from AHA or ...
  • 5/17/2024 12:00:00 AM

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Clinical Research Coordinator
  • American Clinical Research Services
  • Montclair, CA
  • Catalina Research Institute (CRI), an ACRS company is located in Montclair, CA and they focus on Phase I-III clinical tr...
  • 5/17/2024 12:00:00 AM

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Clinical Research Coordinator
  • North America Research Institute
  • San Dimas, CA
  • Job Description Job Description Seeking professional individual capable of managing study progress for multiple trials, ...
  • 5/16/2024 12:00:00 AM

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Clinical Research Coordinator - 220815
  • Medix™
  • Los Angeles, CA
  • Duration: 3 month contract Schedule: 40 hours per week (Monday through Friday 8AM-5PM EST) Location: 90057 Los Angeles, ...
  • 5/16/2024 12:00:00 AM

Income Estimation for Clinical Research Coordinator jobs
$60,215 to $81,190

Career Path for Clinical Research Coordinator