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    PS

    Psi Cro

    Clinical Research

    Site Management Associate I

    Buenos Aires, ArgentinaHybridFull-timePosted 3d ago
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    Job description

    Join our international team and be the key support to clinical research projects, streamlining communication, maintaining systems and managing documents & information.

    Only CVs in English will be accepted.

    You will be responsible for:

    • Being the main point of contact between site personnel and CRA involved in the project helping on query resolution and EDC completion.
    • Serves as the primary sites’ contact point for vendors, study supplies, and access management.
    • Ensure that pre-study testing (scans, MRI/CT qualification questionnaires, test ECGs, etc.) of local site facilities is completed.
    • Assists the Monitors in their prompt completion of all subject event and site event information in CTMS. Track the resolution status of site issues and action items in CTMS.
    • Act as the one who will ensure the order, receipt, inventory storage, distribution, return/recall and reconciliation of clinical supplies.
    • Ensures regulatory and ethics committee submissions and notifications, meaning you will need to be up to date on local regulations and dispositions.
    • Coordinate preparation for and follow-up on site, TMF and systems´ audits and inspections.
    • Manage the TMF on a site and a country level for regularly and file documents. Prepare, distribute, and update Investigator Site Files (ISF) and ISF checklists.
    • Arrange and track initial and on-going project training for site teams in all vendor-related systems.
    • Document Management and translations status review of the study.
    • Ensures proper safety information flow with investigative sites.
    • College/University Degree in Life Sciences;
    • Administrative work experience, preferably in an international settings;
    • Prior experience working as CTA for CROs;
    • Prior experience working in Clinical Research;
    • Local regulations knowledge;
    • Full working proficiency in English;
    • Proficiency in MS Office applications;
    • Ability to plan and work in a dynamic team environment;
    • Communication and collaboration skills.

    Advance your career in clinical research, coordinating a variety of tasks and learning new things while growing with the company.

    Job details are sourced from the employer's original posting.

    Open job posting
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    About the company

    Psi Cro

    At Milestone One , we’re transforming access to clinical trials by expanding research site networks and fostering strategic partnerships with medical institutions. Our mission is to connect patients, physicians, and sponsors in a seamless ecosystem that accelerates breakthrough treatments. With over 30 years of global experience , we are a team of industry experts dedicated to quality, innovation, and collaboration. As our Operations Manager , you’ll play a key role in driving our business expansion through leading the local team and building strong, long-term partnerships with clinical research organizations and medical institutions.

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    Industry
    Clinical Research
    Open roles
    170

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