Clinical Research Coordinator jobs in Conway, AR

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 (CRC)
  • EVOLUTION RESEARCH GROUP
  • Little Rock, AR OTHER
  • Job Details

    Job Location:    LOC023 WIRG Woodland International Research Group - Little Rock, AR
    Salary Range:    Undisclosed

    CRC

    Title: Clinical Research Coordinator 

    Location: WIRG

    About us:

    ERG is a leading U.S. based, privately held, independent clinical research site company, and provider of clinical development services with expertise in early and late-stage neuroscience drug development. With 20 wholly owned clinical sites and 4 affiliated sites, we conduct in-patient and out-patient phase I-IV clinical research studies. ERG has 400 in-patient beds, a large and growing database of patients suffering from mental illness, neurological disorders, sleep disorders, addictions, Acute and Chronic Pain, diabetes, and other illnesses as well as normal healthy volunteers who participate in trials for the advancement of medicine. With access to over 32 million patients/subjects and 5000 completed trials, ERG continues to grow its capabilities and expand into indications where there are tremendous unmet medical needs in the United States and globally.

    Job Description:

    The Clinical Research Coordinator is responsible for the overall coordination, organization, management, and efficient implementation of clinical trials. The CRC completes all study related procedures and distributes study medication and instructions to research subjects under the direction of the Principal Investigator and the Site Director. They maintain accurate, confidential files and documentation of study participants. In executing these position responsibilities, the Clinical Research Coordinator is guided by FDA regulations, Good Clinical Practice (GCP), and company standard operating procedures and policies.

    Responsibilities:

    General

    • Obtain detailed knowledge of all components of each study protocol through review and analysis of study information with Principal Investigator and Site Director prior to the effective date of the study.
    • Assist to develop draft source documents and review the documents for accuracy and clarity prior to study start up.
    • Review with Principal Investigator and Site Director, any components of the study for which additional information or clarification are required prior to the initiation of the study.
    • Manage studies with direct oversight from Site Director, and Principal Investigator to ensure compliance with protocol requirements.
    • Manage studies with Principal Investigator, Site Director, and Recruitment Manager to develop effective programs for study enrollment.
    • Contribute to the SOP review and development as delegated by the Site Director.

    Study Management

    • Perform study activities as delegated by the Principal Investigator and under the supervision of the Site Director.
    • Attend the investigator meeting for each assigned protocol, as appropriate with directive from Site Director.
    • In conjunction with Site Director and Principal Investigator, ensure adherence to the protocols and document breaches or violations with sponsors and appropriate Institutional Review Boards (IRBs) and other outside regulatory organizations, as required.
    • Screen, enroll subjects and schedule subject visits in conjunction with Principal Investigator
    • Review and obtain informed consent from with potential study volunteer
    • Document all written and phone correspondences with sponsor, labs, IRB other regulatory organizations
    • Maintain organized, accurate and complete study records
    • Assist Principal Investigator in conducting studies in manner to ensure integrity of data and safety of subjects.
    • Enter data as appropriate for protocol (paper-electronic data capture)
    • In conjunction with Principal Investigator, accurately report and track adverse events as defined by each study protocol.
    • Perform study close-out procedures.
    • Store study records appropriately
    • Additionally, this role may encompass responsibilities beyond those outlined above, as required by the evolving needs of the organization. This job description is intended as a foundation and may be subject to expansion or modification to best suit ERG’s objectives.

    Skills and Qualifications:

    • Education and experience
      • High School Diploma or its equivalent; College degree preferred.
      • Able to communicate with providers, co-workers, sponsors, and others in a collaborative and courteous manner.
      • Knowledgeable in medical terminology to communicate with physician office and laboratory staff.
      • Demonstrate the initiative to act independently, initiate activity as required and make appropriate decisions within the constraints of study protocols, regulatory requirements, and company policy.
      • Able to initiate or modify behavior to achieve desired outcomes in spite of environmental factors, priorities, or problems that might not be well defined or that are subject to change.
    • Requirements
      • Understand regulatory requirements, as well as Good Clinical Practices (GCP) and International Conference of Harmonization (ICH) guidelines.
      • Excellent communication skills (interpersonal, written, verbal)
      • Basic computer skills to include Word, Excel, as well as proprietary applications unique to the clinical research industry (such as Study Manager)

    Qualifications


  • 14 Days Ago

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Clinical Pathology Coordinator ASCP
  • Clinical Management Consultants
  • Little Rock, AR FULL_TIME
  • Are you ready to take your career to new heights? An exciting opportunity awaits you at one of Central Arkansas's premier hospitals, recognized for its excellence and innovation in healthcare. We are ...
  • 1 Month Ago

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Salon Coordinator
  • Sport Clips - Coordinator - AR101
  • Little Rock, AR FULL_TIME
  • Sport Clips is seeking a dynamic and enthusiastic Salon Coordinator to join our team and play a pivotal role in delivering exceptional customer service and ensuring the smooth operation of our salon. ...
  • 1 Month Ago

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Salon Coordinator
  • Sport Clips - Coordinator - AR107
  • Hot Springs, AR FULL_TIME
  • Sport Clips is seeking a dynamic and enthusiastic Salon Coordinator to join our team and play a pivotal role in delivering exceptional customer service and ensuring the smooth operation of our salon. ...
  • 1 Month Ago

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Research Coordinator
  • Arkansas Dermatology
  • North Little Rock, AR FULL_TIME
  • Company:Arkansas Research TrialsDermatology clinical research center seeking a skilled professional to assist with clinical trials, regulatory duties, and general research practices. Looking for a hig...
  • 23 Days Ago

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Safety Claims Coordinator
  • Safety Claims Coordinator
  • Little Rock, AR FULL_TIME
  • At CalArk, we respect what you have to offer. Our industry-leading wages and benefits ensure you always feel appreciated for what you individually bring to our team. Your talent has a home with us.
  • 1 Day Ago

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0 Clinical Research Coordinator jobs found in Conway, AR area

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Licensed Talk Therapist
  • Thriveworks
  • Conway, AR
  • Thriveworks is currently seeking Licensed Clinicians to provide a mix of telehealth and face-to-face sessions in Conway,...
  • 3/28/2024 12:00:00 AM

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Clinical Social Worker
  • Thriveworks
  • Conway, AR
  • Thriveworks is currently seeking Licensed Clinicians to provide a mix of telehealth and face-to-face sessions in Conway,...
  • 3/28/2024 12:00:00 AM

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Clinical Research Nurse
  • CARTI, Inc.
  • Little Rock, AR
  • Description Job Summary: The Clinical Research Nurse (CRN) executes and coordinates daily clinical research activities a...
  • 3/28/2024 12:00:00 AM

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Licensed Practical Nurse
  • Department of Veterans Affairs
  • Conway, AR
  • Summary This is an OPEN CONTINUOUS ANNOUNCEMENT and will remain open until September 30, 2024 or until all positions are...
  • 3/28/2024 12:00:00 AM

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Part Time Licensed Talk Therapist
  • Thriveworks
  • Conway, AR
  • Thriveworks is currently seeking Licensed Clinicians to provide a mix of telehealth and face-to-face sessions in Conway,...
  • 3/28/2024 12:00:00 AM

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Licensed Psychologist
  • Thriveworks
  • Conway, AR
  • Thriveworks is currently seeking Licensed Clinicians to provide a mix of telehealth and face-to-face sessions in Conway,...
  • 3/28/2024 12:00:00 AM

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Licensed Psychologist
  • Thriveworks
  • Conway, AR
  • Thriveworks is currently seeking Licensed Clinicians to provide a mix of telehealth and face-to-face sessions in North L...
  • 3/28/2024 12:00:00 AM

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Part Time Licensed Talk Therapist
  • Thriveworks
  • Conway, AR
  • Thriveworks is currently seeking Licensed Clinicians to provide a mix of telehealth and face-to-face sessions in Conway,...
  • 3/27/2024 12:00:00 AM

Conway is a city in the U.S. state of Arkansas and the county seat of Faulkner County, located in the state's most populous Metropolitan Statistical Area, Central Arkansas. Conway is unusual in that the majority of its residents do not commute out of the city to work. The city also serves as a regional shopping, educational, work, healthcare, sports, and cultural hub for Faulkner County and surrounding areas. Conway's growth can be attributed to its jobs in technology and higher education with its largest employers being Acxiom, the University of Central Arkansas, Hewlett Packard, Hendrix Coll...
Source: Wikipedia (as of 04/11/2019). Read more from Wikipedia
Income Estimation for Clinical Research Coordinator jobs
$54,943 to $74,070
Conway, Arkansas area prices
were up 1.2% from a year ago

Clinical Research Coordinator in Monterey, CA
Coordinators often become the front line for patients because they feel more comfortable with us.
November 07, 2019
Clinical Research Coordinator in Bakersfield, CA
If you have a medical experience you may need a certificate program to work as a CRC bt if there is none then you will need an education program that covers all the required medical and research coursework in clinical research.
October 27, 2019
Clinical Research Coordinator in New Bedford, MA
If you’re looking for a job you can complete at home that lets you use your organizational and leadership skills, a career in clinical research coordination could be for you.
October 09, 2019