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Clinical Research Coordinator

Company: Medix
Location: Anderson
Posted on: January 16, 2022

Job Description:

Medix is Hiring!
We are seeking a Clinical Research Coordinator for a growing Site Management Organization (SMO) in the Anderson,SC area to join our team immediately.
They are offering Relocation Assistance or a Sign on Bonus if you currently live in Anderson, SC!!
Clinical Research Coordinator Position Summary:

  • Coordinate all aspects of clinical research trials, ensures compliance with protocols, ensure regulatory compliance, liaison with monitors and sponsors, schedule visits for subjects and communicate effectively with Director of Clinical Operations /Site Director, Principal Investigators and Sub-Investigators. Must be able to work independently and handle multiple tasks. Must be able to work overtime if needed. Must be available to be 'on-call' as assigned.
    Clinical Research Coordinator Responsibilities:
    • Coordinate and participate in protocol assessment and site preparation for study initiation. Includes the ability to evaluate protocols for feasibility and recruitment strategies.
    • Ensure the safety and welfare of all study subjects.
    • Ensure compliance with multiple assigned protocols. Must successfully conduct all assigned protocols in accordance with FDA, RMR SOPs and ICH GCP guidelines.
    • Assure IRB approval obtained prior to beginning any procedures.
    • Develop, coordinate and implement research and administrative strategies to successfully manage assigned protocols.
    • Recruit subjects for all assigned protocols within timelines given by Director of Clinical Operations /Site Director Responsible for knowing target goal for enrollment and enrollment period.
    • Proficient with phlebotomy and infusions.
    • Properly consent subjects in accordance with FDA, GCP and protocol guidelines. Must work closely with the Principal Investigator to ensure proper subject enrollments through thorough understanding of inclusion and exclusion criteria for each protocol. Assure Investigator approval of subject enrollment prior to randomization including review of all safety data. Accurately record all adverse events and concomitant medications on each subject. Ensure timely review of all adverse events by appropriate Investigator.
    • Schedule and oversee all subject visits on assigned protocols. Schedule all visits within proper time window as set forth in assigned protocols. Ensure subject safety in conjunction with Investigators; communicate and get proper signatures on safety data in a timely manner.
    • Track enrollment of each study. Communicate enrollment targets, goals, and strategies with investigators, sponsors, monitors and Director of Clinical Operations /Site Director as appropriate.
    • Collect and accurately record study data in source documents and case report forms.
    • Design and maintain organizational tools to conduct the study accurately and in compliance with GCP, FDA and protocol guidelines.
    • Complete all paperwork as required by sponsor and RMR guideline.
    • Train other site personnel and medical staff in understanding and implementation of assigned protocols.
      Clinical Research Coordinator Qualifications:
      • Clinical Research Coordinator experience would be ideal
      • Demonstrates interpersonal and collaboration skills
      • Superior verbal and written communication skills
      • Strong computer skills are required, especially in Excel and data analysis; skilled with the Microsoft Office Suite and comfortable navigating web-based programs
        Benefits:Once you have been a contract employee of Medix for 30 days, you become eligible for our Benefits Program. Should you elect to enroll, there are three levels of medical coverage to choose from, supplemental dental plans and term plans as well as the option to enroll your spouse and/or children. You can select the best combination that best suits your needs.
        As a contract employee with Medix, you can choose to enroll in our Benefits Program during your eligibility period and enjoy:
        401(k) Retirement PlanPaid time off benefits availableA limited benefit medical plan with the American WorkerDoctor visits with inexpensive co-payLimited Outpatient CareLimited Accident CoveragePrescription ProgramsDental PlanVision Discount ProgramTerm Life Insurance PlansMedix is dedicated to positively impacting lives every day!This years recipient of the Business Ledger's 'Entrepreneurial Excellence Growth Award'Join our network of talented professionals!
        Compensation: Dependent upon experience
        Apply Today!by Jobble

Keywords: Medix, Athens , Clinical Research Coordinator, Healthcare , Anderson, Georgia

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