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    PS

    Psi Cro

    Clinical Research

    Site Management Associate II

    Durham, United StatesHybridFull-time2+ yrs experiencePosted 1w ago
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    Job description

    Start your career in clinical research, streamlining communication, maintaining systems and managing documents.

    The scope of responsibilities will include:

    • Main site contact for all non-trial-participant related and non-protocol related issues, including vendors, trial supplies and access management
    • Manages records flow with sites and off-site facilities
    • Prepares regulatory and ethics committee submission/ notification documents and records
    • Coordinates payments to sites and off-site facilities
    • Prepares for and follows up on site audits and inspections
    • Reviews and coordinates site-specific query resolution with Monitors and sites
    • Reviews site-specific EDC completion progress and provides the Monitor with regular updates
    • Serves as the main contact point for other company departments in administrative site-related issues
    • Organizes, participates in, and prepares reports of internal project team meetings
    • Collaborates with sites and project team on Investigator Meetings'
      organization
    • Under supervision, provides on-the-job coaching of Site Management
      Associates I and Clinical Operations Administrative Support staff
    • Arranges and tracks initial and ongoing trial training for investigator site teams in all vendor-related systems
    • Provides training in courier management and trial supplies ordering to the investigator sites
    • Files trial records in the TMF and performs regular TMF checks on a site and country level
    • Participates in and follows up on TMF and systems audits
    • Prepares, distributes, and updates Investigator Site Files (ISF) and ISF checklists
    • Coordinates the translation process for trial records on a site and country level
    • Collects IP-REDs and compiles IP-RED packages for further review
    • College or university degree or an equivalent combination of education, training and experience that presents the required knowledge, skills and abilities is considered sufficient.
    • Minimum 2 year experience within the clinical research industry, corporate or academic environment where administrative experience and technical skills have been gained.
    • Basic proficiency in MS Word.
    • Basic proficiency in MS Excel.
    • Basic proficiency in MS Outlook.
    • Basic proficiency in MS Power Point.
    • Knowledge (following proper training) of applicable software and project specific systems.
    • Basic typing skills in English (min. 40 words per minute)

    Make the right call and take your career to a whole new level. Join the company that focuses on its people and invests in their professional development and success.

    For this position, PSI is not hiring individuals who require work visa for employment or continued employment now or anytime in the future.

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

    Open job posting
    PS

    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.

    View all Psi Cro jobs
    Industry
    Clinical Research
    Open roles
    117

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