Jobs

    CRA (Ophthalmology) - Texas, United States - Randstad Life Sciences

    Randstad Life Sciences
    Randstad Life Sciences Texas, United States

    2 days ago

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    Description

    We are looking for a Clinical Research Associate with Ophthalmology Experience!

    Join our team for a 2-Year Contract with a Pay Rate of $75-85/hour.

    This position is location flexible - you can work remotely! However, keep in mind that candidates need to be in specific states like CA, AZ, IL, WA, NC, FL, SC, GA, NY, TX, MA.

    Job Description:

    • As a Contract CRA specialized in ophthalmology, you will monitor and manage clinical trials related to eye diseases, ophthalmic treatments, and devices at various sites. Your main goal is to ensure that these trials are conducted in compliance with all necessary guidelines and protocols.

    Main Responsibilities:

    • Site Selection and Initiation:
    • Assist in selecting investigative sites for trials.
    • Conduct site initiation visits to ensure proper staff training, regulatory compliance, and understanding of protocols.
    • Monitoring and Site Management:
    • Perform on-site and remote visits to monitor data quality and compliance.
    • Review documents and patient records.
    • Regulatory Compliance:
    • Ensure sites comply with regulatory requirements.
    • IP and Clinical Supplies Oversight:
    • Verify subject qualification and proper product dispensing.
    • Data Management:
    • Verify data accuracy and collaborate with the data management team.
    • Safety Reporting:
    • Communicate safety issues according to requirements.
    • Close-Out Visits:
    • Finalize data collection and ensure study completion.
    • Documentation and Reporting:
    • Complete monitoring reports and maintain documentation up to date.

    Requirements:

    • Bachelor's degree in life sciences or nursing.
    • Prior experience as a Clinical Research Associate, preferably in ophthalmology.
    • Knowledge of ophthalmic diseases and related medical terminology.
    • Understanding of clinical research regulations and Good Clinical Practice guidelines.
    • Strong communication and interpersonal skills.
    • Attention to detail and ability to work independently or in a team.
    • Willingness to travel for monitoring visits.
    • Certification as a Clinical Research Associate is a plus.


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