Clinical Research Manager jobs in Conway, AR

Clinical Research Manager manages the clinical monitoring process and the administration of clinical trials. Supervises CRAs in in-house and on-site monitoring, filing, and clinical trial administration. Being a Clinical Research Manager oversees adherence to SOPs, Good Clinical Practice and FDA regulations. Helps with the development and implementation of clinical processes, procedures, and programs. Additionally, Clinical Research Manager may require a master's degree in nursing. May require ACRP or SOCRA Clinical Research Professional exam completion. Typically reports to a director. The Clinical Research Manager manages subordinate staff in the day-to-day performance of their jobs. True first level manager. Ensures that project/department milestones/goals are met and adhering to approved budgets. Has full authority for personnel actions. To be a Clinical Research Manager typically requires 5 years experience in the related area as an individual contributor. 1-3 years supervisory experience may be required. Extensive knowledge of the function and department processes. (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


  • 15 Days Ago

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Clinical Research Monitoring Specialist
  • University of Arkansas
  • Little Rock, AR FULL_TIME
  • Current University of Arkansas System employees, including student employees and graduate assistants, need to log in to Workday via MyApps.Microsoft.com, then access Find Jobs from the Workday search ...
  • 15 Days Ago

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Territory Account Manager
  • Syneos Health Clinical
  • Little Rock, AR FULL_TIME
  • Description You have what it takes: a competitive drive coupled with exceptional sales ability. In this role, you will be an integral part of a nationwide sales team developing and managing an assigne...
  • 5 Days Ago

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Staff Clinical Research Associate, Adona Medical
  • Adona Medical
  • Adona, AR FULL_TIME
  • Adona Medical, a Shifamed Portfolio Company, is focused on innovating interventional approaches for heart failure, a complex and progressive condition. Heart failure is a progressive condition that im...
  • 1 Day 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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Assistant Clinical Services Manager
  • University of Arkansas
  • Little Rock, AR FULL_TIME
  • Current University of Arkansas System employees, including student employees and graduate assistants, need to log in to Workday via MyApps.Microsoft.com, then access Find Jobs from the Workday search ...
  • 20 Days Ago

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0 Clinical Research Manager jobs found in Conway, AR area

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Family Nurse Practitioner (ARNP) (FNP)
  • DispatchHealth Management
  • Little Rock, AR
  • How You'll Make an Impact: We are hiring Nurse Practitioners and Physician Assistants with acute care experience in ER, ...
  • 3/28/2024 12:00:00 AM

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RRT II - PRN
  • Arkansas Children's Hospital
  • Little Rock, AR
  • ARKANSAS CHILDREN'S IS A TOBACCO FREE WORKPLACE. COVID AND FLU VACCINES ARE REQUIRED. ARKANSAS CHILDREN'S IS AN EQUAL OP...
  • 3/28/2024 12:00:00 AM

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RN II, 3C Intermediate Care, Weekend Option, Full Time, 7p-7a, $10K Sign On
  • Arkansas Children's Hospital
  • Little Rock, AR
  • ARKANSAS CHILDREN'S IS A TOBACCO FREE WORKPLACE. FLU VACCINES ARE REQUIRED. ARKANSAS CHILDREN'S IS AN EQUAL OPPORTUNITY ...
  • 3/28/2024 12:00:00 AM

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Patient Safety Risk and Education Specialist -- Quality -- Greenbrier Valley Medical Center - 1320 M
  • CAMC Health System
  • Greenbrier, AR
  • Job Summary Responsible for health system risk management and educational activities to facilitate a culture of safety a...
  • 3/27/2024 12:00:00 AM

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Research Associate I/II/III
  • University of Arkansas System
  • Little Rock, AR
  • Current University of Arkansas System employees including student employees and graduate assistants need to log into Wor...
  • 3/26/2024 12:00:00 AM

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Physician Assistant (PA-C)- PRN
  • Dispatchhealth Management
  • Little Rock, AR
  • How You'll Make an Impact: We are hiring Nurse Practitioners and Physician Assistants with acute care experience in ER, ...
  • 3/26/2024 12:00:00 AM

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Family Nurse Practitioner (ARNP) (FNP)
  • Dispatchhealth Management
  • Little Rock, AR
  • How You'll Make an Impact: We are hiring Nurse Practitioners and Physician Assistants with acute care experience in ER, ...
  • 3/26/2024 12:00:00 AM

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Nurse Practitioners (NP/ APRN)- Part-time
  • Dispatchhealth Management
  • Little Rock, AR
  • How You'll Make an Impact: We are hiring Nurse Practitioners and Physician Assistants with acute care experience in ER, ...
  • 3/25/2024 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 Manager jobs
$90,523 to $119,937
Conway, Arkansas area prices
were up 1.2% from a year ago

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