Clinical Research Coordinator jobs in Ohio

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 Assistant
  • Velocity Clinical Research, Inc.
  • Cleveland, OH FULL_TIME
  • Overview

    Velocity Clinical Research is an owned and integrated research site organization, providing excellence in patient care, high quality data and fully integrated research sites. At Velocity, we align our values and behaviors to give our employees the best chance of delivering on our brand promise: to bring innovative medical treatments to patients. We are committed to making clinical trials succeed by generating high quality data from as many patients as possible, as quickly as possible while providing exemplary patient care at every step.

     

    As an employee of Velocity, you are the most integral part of our mission. For talented candidates who perform at a high level, Velocity will invest to support career advancement and reward performance. Whether you are new to clinical research or are an industry veteran, we invite you to apply to Velocity.

     

    Benefits include medical, dental and vision insurance, paid time off and company holidays, 401(k) retirement plan with company-match, and an annual incentive program.

     

    Summary:

    The Clinical Research Assistant assists the Clinical Operations Team in a multi-functional capacity to carry out all assigned tasks associated with the collection, documentation, and maintenance of clinical data including phlebotomy/laboratory, data entry and administrative responsibilities.

    Responsibilities

    Duties/Responsibilities:

    • Assist in the conduct of clinical trials in accordance with the study protocol, GCP, ICH Guidelines, and Velocity’s SOPs
    • Perform venipuncture, capillary puncture and/or other fluid collection within scope of the protocol and local law and regulations
    • With supervision, perform clinical assessments (vital signs, phlebotomy, ECG, etc) within scope of the protocol, local law and regulations
    • Process, package and ship laboratory specimens as required per protocol and IATA regulations, if applicable
    • Track, order and maintain inventory of all laboratory and study related supplies throughout course of the clinical trial
    • Enter source data into the sponsor's and/or vendor’s data portal and resolve basic queries in a timely manner under the direction of the Clinical Research Coordinator
    • Communicate with coworkers, leadership, study subjects, sponsors, CROs, and vendors under the direction of the Clinical Research Team
    • Understand good documentation practices when collecting, transferring data to sponsor/CRO data capture systems and resolving queries under the direction of the Clinical Research Coordinator
    • Understand the informed consent process with emphasis on ensuring initial and ongoing consent of study subjects
    • Understand basic elements of regulatory documentation required to initiate, maintain and close a clinical research trial
    • Understand and participate in patient recruiting tasks including but not limited to prescreening potential subjects for clinical research trials either via phone or in person
    • Maintain confidentiality of patient protected health information, sponsor confidential information and Velocity confidential information
    • Ability to escalate potential patient safety issues such as adverse events, serious adverse events, and adverse events of special interest to the Clinical Research Team
    • Cleaning, organizing, and disinfecting the patient care, lab and lab equipment areas as needed
    • Prepare source document charts, copy and/or file medical records and study related documents as required.
    • Perform front office duties as needed including but not limited to answering phones, scheduling subjects, making reminder calls and updating patient tracking systems.
    • Other duties as assigned

    Qualifications

    Education/Experience:

    • High School Graduate and/or technical degree with minimum of 1 year of relevant experience in life sciences industry

    Required Licenses/Certifications:

    • Phlebotomy if applicable and required by state law
    • Intramuscular dose administration and preparation if applicable and required by state law

    Required Skills:

    • Demonstrated knowledge of medical terminology
    • Demonstrated ability to use the following technology: Computers, Microsoft Office software, fax, copier, and multi-line telephone.
    • Understanding of verbal, written, and organizational skills
    • Demonstrated ability to work as a team player
    • Demonstrated ability to read, write, and speak English
    • Demonstrated ability to multi-task
    • Demonstrated ability to follow written guidelines
    • Demonstrated ability to be flexible/adapt as daily schedule may change rapidly

    Required Physical Abilities:

    • Sit or stand for long periods of time
    • Communicate in person and by a telephone
    • Limited walking required
    • Limited to lifting up to 30 pounds

    NOTE: The above Job Description is intended to communicate the general function of the mentioned position and by no means should be considered an exhaustive or complete outline of the specific tasks and functions that will be required.  Additionally, specific tasks and duties of the position are subject to change as the Company, the department and circumstances change.  All employees are expected to perform their duties within their ability as required by the job and/or as requested by management.

     

  • 13 Days Ago

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Clinical Research Assistant
  • Velocity Clinical Research, Inc.
  • Cincinnati, OH PER_DIEM
  • Overview Velocity Clinical Research is an owned and integrated research site organization, providing excellence in patient care, high quality data and fully integrated research sites. At Velocity, we ...
  • 16 Days Ago

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Clinical Research Assistant
  • Velocity Clinical Research, Inc.
  • Mount Auburn, OH FULL_TIME
  • Overview Velocity Clinical Research is an owned and integrated research site organization, providing excellence in patient care, high quality data and fully integrated research sites. At Velocity, we ...
  • 1 Month Ago

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Director, Clinical Site
  • Velocity Clinical Research, Inc.
  • Cleveland, OH FULL_TIME
  • Overview Velocity Clinical Research is an owned and integrated research site organization, providing excellence in patient care, high quality data and fully integrated research sites. At Velocity, we ...
  • 20 Days Ago

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Clinical Research Coordinator
  • ObjectiveHealth
  • Woodway, TX
  • Clinical Research Coordinator Our clinical research company is looking to hire a qualified candidate for the full-time p...
  • 3/29/2024 12:00:00 AM

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Clinical Research Coordinator
  • Northwest Georgia Oncology Centers, PC
  • Hiram, GA
  • Job Description Job Description Busy oncology practice has an immediate opening for a FT Clinical Research Coordinator. ...
  • 3/29/2024 12:00:00 AM

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Clinical Research Coordinator
  • NYU Langone Health
  • New York, NY
  • NYU Grossman School of Medicine is one of the nation's top-ranked medical schools. For 175 years, NYU Grossman School of...
  • 3/28/2024 12:00:00 AM

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Clinical Research Coordinator
  • Sanford Health
  • Fargo, ND
  • Create Your Career With Us! Sanford Health is one of the largest and fastest-growing not-for-profit health systems in th...
  • 3/28/2024 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 ...
  • 3/28/2024 12:00:00 AM

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Clinical Research Coordinator
  • Danbury Health Systems
  • Poughkeepsie, NY
  • Full Time Clinical Research Coordinator Opportunity - Poughkeepsie, NY (75 Miles from New York City) Nuvance Health has ...
  • 3/28/2024 12:00:00 AM

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Clinical Research Coordinator
  • Beth Israel Lahey Health
  • Boston, MA
  • When you join the growing BILH team, you're not just taking a job, you're making a difference in people's lives. Job Typ...
  • 3/27/2024 12:00:00 AM

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Clinical Research Coordinator
  • CARLE
  • Peoria, IL
  • Promotes good clinical practices in the conduct of clinical investigations by possessing an in-depth knowledge of federa...
  • 3/26/2024 12:00:00 AM

Ohio /oʊˈhaɪoʊ/ (listen) is a Midwestern state in the Great Lakes region of the United States. Of the fifty states, it is the 34th largest by area, the seventh most populous, and the tenth most densely populated. The state's capital and largest city is Columbus. The state takes its name from the Ohio River, whose name in turn originated from the Seneca word ohiːyo', meaning "good river", "great river" or "large creek". Partitioned from the Northwest Territory, Ohio was the 17th state admitted to the Union on March 1, 1803, and the first under the Northwest Ordinance. Ohio is historically know...
Source: Wikipedia (as of 04/11/2019). Read more from Wikipedia
Income Estimation for Clinical Research Coordinator jobs
$58,929 to $79,444

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