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Clinical Research Coordinator
Clinical Research CoordinatorSalma Mazhar MD PA • Mesquite, TX, US
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Clinical Research Coordinator

Clinical Research Coordinator

Salma Mazhar MD PA • Mesquite, TX, US
[job_card.30_days_ago]
[job_preview.job_type]
  • [job_card.full_time]
[job_card.job_description]

Job Description

Job Description

Benefits :

  • Dental insurance
  • Health insurance
  • Opportunity for advancement
  • Paid time off
  • Profit sharing
  • Tuition assistance
  • Vision insurance

EXPERIENCE IN CLINICAL RESEARCH IS A MUST

The Clinical Research Coordinator is responsible for managing the daily operations of a clinical investigation. This position will manage multiple, sponsored (Phase I, II, III, IV, and V) clinical trials for many indications within primary care.

The Essential Job Functions are :

  • Maintain a detailed knowledge of all study protocols in order to complete all study activities correctly and completely
  • Recruit and screen patients for assigned studies
  • Provide instructions and education to subjects to ensure proper protocol compliance
  • Complete visit procedures including, but not limited to, obtaining vital signs measurements, performing ECG's, and collecting blood samples for processing and shipment to the appropriate lab facility
  • Notify the Investigator of all adverse events
  • Report all serious adverse events in compliance with FDA regulations and sponsor requirements
  • Provide the Sponsor with accurate and complete documentation and information
  • Complete and maintain accurate, legible and complete source documents and case report forms per FDA guidelines and Sponsor requirements
  • Prepare for FDA audit by ensuring all documentation and case report forms are available and complete. Ensure the rights, safety and welfare of all subjects at all times
  • Ensure that each subject has completed the informed consent process, following GCP guidelines, and has consented to participate before any study related procedures are performed
  • Provide subjects education on an ongoing basis throughout their participation in the protocol
  • Report all adverse events to the Investigator, Sponsor and IRB
  • Complete all relevant site-level and study-level logs in a timely manner
  • Utilize a team approach including the PI, Sub-Investigators, Site Manager, other Coordinators and Research Assistants
  • Act as a liaison to ensure complete and accurate communication between physicians, sponsors and subjects. Work in a collaborative, effective manner with the Sponsor to meet research objectives
  • Understand all internal policies and procedures approved by the Medical Director, Site Manager, and any other departments

    • Job Type : Full-time

    Experience :

  • Clinical research coordinator : 2 year (Required)
  • Phlebotomy : 1 year (Required)
  • Vital Signs : 1 year (Required)

    • Education :

  • High school or equivalent (Required)

    • License :

  • CCRC / CCRP (Preferred)
    • [job_alerts.create_a_job]

    Clinical Research Coordinator • Mesquite, TX, US

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