Clinical Research Coordinator jobs in Nevada

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 (Entry Level)
  • Wake Research
  • Enterprise, NV FULL_TIME
  • Job Description

    We are looking for an entry level Clinical Research Coordinator (CRC) to join our growing team. This position is fully on-site.

    The Clinical Research Coordinator (CRC) is a specialized research professional working with, and under the direction of, the clinical research site management and Principal Investigator (PI). While the PI is primarily responsible for the overall conduct of the clinical trial, the CRC manages, supports, facilitates, and coordinates the daily trial activities and plays a critical role in the conduct of the study. By performing these duties, the CRC works with the PI, sponsor, and clinical trial site to support and ensure compliance related to all aspects of the clinical study. The primary concern of all Wake Research personnel is the protection of the study subjects.

    Essential Duties and Responsibilities:

    Completes all site training requirements, including but not limited to, GCP training, IATA training, OSHA training, site SOP review, and individual department training.

    Cooperates with site management and monitoring efforts to ensure protocol adherence. Reports instances of non-compliance, external inspections/audits immediately to site management.

    Coordinates with site management/PI to help ensure that clinical research protocol and related activities are performed in accordance with ICH/GCP, federal regulations, Research site SOPs and sponsoring agency policies and procedures.

    Reviews and adheres to assigned protocol, e.g., study procedures and timelines, inclusion and exclusion criteria.

    Attends investigator meetings for assigned studies as required. Some travel may be required.

    Maintains organized study files, including but not limited to regulatory binders, source documents and other materials.

    Attends PSVs, SIVs, IMVs, and COVs as required.

    Begins to learn process of regulatory duties as they relate to coordination of clinical trials, to include, but not limited to: Providing appropriate study training tools for study team members with appropriate documentation, maintenance and completion of Delegation of Authority Log, sponsor and vendor communication documents, IP/device documentation, etc.

    Assist with recruitment strategies and collaborate with recruitment department to ensure suitable subjects meet study criteria and enrolment goals are met.

    In accordance with site’s informed consent SOP, participates in the informed consent process with research participants by confirming ICF was executed and documented appropriately.

    Performs study-related procedures that have been trained/delegated by PI according to study protocol (i.e. vital signs, EKG, phlebotomy, pulmonary function testing, urine pregnancy and drug testing, processing blood, or any other procedures required per protocol or ordered by study investigator) and documents appropriately on source documents.

    Assists with timely completion of case report forms, if appropriately delegated/trained.

    Maintains adequate inventory of all study supplies. When handling investigational drugs/devices, follows the protocol for Investigational Drug/Device Accountability.

    When required, has professional and ongoing communication with sponsor, sponsor representatives, research participants and investigators during the study and documents accordingly.

    Assists fellow co-workers with studies as time and ability permits or as management delegates.

    Schedules secure storage of study documents with management once close-out visit has been performed and reconciliation of all study documents has occurred.

  • 15 Days Ago

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Clinical Research Coordinator- Twain
  • The US Oncology Network
  • LAS VEGAS, NV OTHER
  • Overview:Comprehensive Cancer Centers of Nevada (CCCN) is dedicated to advancing cancer care by leading and participating in many clinical research studies in Nevada that test the safety and efficienc...
  • Just Posted

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Clinical Research Coordinator (Entry Level)
  • M3USA
  • Las Vegas, NV FULL_TIME
  • Company DescriptionM3 Wake Research is an integrated network of premier investigational sites meeting the clinical research needs of global biopharmaceutical, biotechnology, medical device, pharmaceut...
  • 12 Days Ago

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Clinical Research Coordinator (On-Site, Las Vegas NV)
  • IQVIA
  • Las Vegas, NV FULL_TIME
  • Job Description:We are seeking a dedicated and efficient Clinical Research Coordinator (CRC) to join our healthcare team. The ideal candidate will be responsible for coordinating clinical research stu...
  • 9 Days Ago

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Travel Clinical Research Coordinator, US Based (Las Vegas, NV)
  • Care Access
  • Las Vegas, NV FULL_TIME
  • What We Do Care Access is delivering the future of medicine today! Care Access has a revolutionary model that breaks down traditional barriers to clinical trials that limit participation among physici...
  • Just Posted

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Nurse Practitioner (NP) - Clinical Research Coordinator - Las Vegas, NV
  • The IMA Group
  • Las Vegas, NV FULL_TIME
  • Company Overview: The Clinical Research Division at The IMA Group is a dynamic hub of expertise and innovation, dedicated to advancing healthcare through clinical trials and studies. Our team of seaso...
  • 4 Days Ago

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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
  • 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
  • Mayo Clinic Health System
  • Rochester, MN
  • Why Mayo Clinic Mayo Clinic is top-ranked in more specialties than any other care provider according to U.S. News & Worl...
  • 3/28/2024 12:00:00 AM

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Clinical Research Coordinator
  • Methodist Healthcare
  • San Antonio, TX
  • Description Introduction Are you looking for a work environment where diversity and inclusion thrive? Submit your applic...
  • 3/28/2024 12:00:00 AM

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Clinical Research Coordinator
  • University of Miami Miller School of Medicine
  • Miami, FL
  • Current Employees: If you are a current Staff, Faculty or Temporary employee at the University of Miami, please click he...
  • 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

Nevada is almost entirely within the Basin and Range Province, and is broken up by many north-south mountain ranges. Most of these ranges have endorheic valleys between them, which belies the image portrayed by the term Great Basin. Much of the northern part of the state is within the Great Basin, a mild desert that experiences hot temperatures in the summer and cold temperatures in the winter. Occasionally, moisture from the Arizona Monsoon will cause summer thunderstorms; Pacific storms may blanket the area with snow. The state's highest recorded temperature was 125 °F (52 °C) in Laughlin (e...
Source: Wikipedia (as of 04/11/2019). Read more from Wikipedia
Income Estimation for Clinical Research Coordinator jobs
$60,734 to $81,876

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