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Site Administrator

Key Facts

Remote From: 
Oregon (USA)
Full time
Junior (1-2 years)
English

Other Skills

  • Data Reporting
  • Microsoft Office
  • Accountability
  • Communication
  • Time Management
  • Teamwork
  • Organizational Skills
  • Detail Oriented
  • Problem Solving

Roles & Responsibilities

  • High school diploma or equivalent
  • At least 1 year of experience in a clinical research setting with proficiency in clinical terminology
  • Experience with site feasibility assessments and identifying study opportunities across multiple therapeutic areas
  • Experience with initial IRB submission and maintenance procedures, and knowledge of GCP

Requirements:

  • Support sponsor/CRO-site coordination for study start-up and site selection, including organizing feasibility information
  • Assist with data entry of clinical trial information, scheduling participant visits and follow-ups, and maintaining regulatory files
  • Maintain up-to-date study documentation, including staff credentials and SOPs; communicate updates to onsite staff
  • Ensure study activities comply with GCP and IRB requirements; assist in preparing study materials, reports, and attending meetings and trainings

Job description

Company Description

We are a fast-growing Site Enabling Organization operating globally in the field of clinical research. We are driven by quality, teamwork, and innovation. As we continue to expand our global operations, we are seeking a passionate and dedicated Site Administrator to join our Operations Team.

    Job Description

    The Site Administrator is an integral part of the SEO Operations team and supports the daily operations of clinical trials, supporting onsite and remote Milestone One staff as assigned. Study-specific delegated tasks will be determined by the Principal Investigator (if applicable), considering all local and federal laws and regulations and upon review of competencies observed and documented by Milestone One. In addition, administrative tasks may be assigned by the Milestone One Manager.

    In this job you will:

    Support the connection between sponsors and/or CROs with appropriate studies and clinical research sites, contributing to study start-up and site selection processes.

    Responsibilities will include providing study site identification support, assisting with the organization and coordination of feasibility-related information, and contributing to process organization and documentation to support operational efficiency.

    Additionally, you may also be asked to assist with the coordination and execution of clinical research studies in compliance with protocols and research regulations.

    • Assist with data entry of clinical trial information as assigned.
    • Assist in scheduling participant visits, coordinating appointments, and follow-ups.
    • Maintain accurate and up-to-date study documentation, including staff credentials and regulatory files. Must be effectively communicate with onsite staff regarding updated documents that impact study data.
    • Maintain files for SOP’s and other internal files as delegated.
    • Ensure all study activities follow Good Clinical Practice (GCP) guidelines and institutional review board (IRB) requirements.
    • Prepare and organize study materials, equipment, and supplies.
    • Support the research team in compiling reports and preparing data for analysis.
    • Attend study meetings and training sessions as required.

    The Site Administrator reports to the Milestone One Manager responsible for the region. Within clinical trials, the Site Administrator reports to the individual Principal Investigator by the responsibilities as delegated on the delegation of authority log for each clinical trial (if applicable). The scope of the Site Administrator’s responsibilities will be clearly defined for each project. The Site Administrator is responsible for providing services as assigned and should consult the Milestone One manager assigned for any questions. 

    Qualifications

    Education

    High school degree or equivalent

    Certifications

    • Current Good Clinical Practice (GCP) may be obtained during orientation
    • International Air Transport Association (IATA) if required, may be obtained during orientation
    • Cardiopulmonary Resuscitation (CPR) if required, may be obtained during orientation

    Experience

    Experienced in a clinical research setting for at least 1 year.  Must demonstrate clinical research and general medical terminology proficiency.

    Proven experience conducting site feasibility assessments, including the ability to develop and execute strategies for identifying study opportunities across multiple therapeutic areas.

    Must have experience with initial IRB submission and maintenance requirements and procedures.  

    Knowledge & Skills

    • Interested in clinical research and healthcare.
    • Strong organizational and time-management skills.
    • Attention to detail and the ability to interpret and implement protocol and guidelines.
    • Proficiency in MS Office
    • Valid category B driver’s license

    Behavioral Skills

    • Excellent communications skills
    • Attention to detail
    • Effective problem-solving and result-oriented
    • Accountability
    • Team player

    Additional Information

    Trainings

    • Induction training in SOPs and admin practices for Site Administrator
    • On-the-job training under the supervision of the SEO Manager or designated person

    Location: Remote (Central or Eastern Time Zone)

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