Clinical Site Coordinator

Vienna, Vienna, at on site Until 8/22/2026 First posted March 13, 2026 Last posted March 13, 2026
Job description

Milestone One is a Site Enabling Services organization with global headquarters in Zug, Switzerland. We understand what clinical study sites need and our overall mission is to support sites in stronger study delivery.

    The Milestone One Site Coordinator role supports a Clinical Study Site in clinical trial related activities according to ICH-GCP, protocol requirements within Study specific defined timelines and enrollment goals.

    The function of the role may include, but not limited to, any/all of the following:

    • Act as the main line of communication between the Sponsor or CRO and the site.
    • Ensure response to feasibility questions are provided in due time.
    • Assist in scheduling and preparation for all types of monitoring visits at the medical institution/research center.
    • Be present and available to respond to monitors during all types of monitoring visits conducted at the medical institution.
    • Track patient enrollment and actively support the medical site and CRO/Sponsor team in meeting project timelines and enrollment goals.
    • Maintain study specific and general tracking of documents at the site level.
    • Accurate and timely data entry into study specific EDC systems and timely resolution of data clarification queries issued for the site.
    • Timely reporting and follow up on Reportable Adverse Events and Protocol Deviations.
    • Proper handling, accountability and reconciliation of investigational products and clinical supplies.
    • Collect, handle and maintain all site-specific regulatory documents as needed.
    • Facilitate and support the contract and budget negotiations at the site level.
    • Support Investigator and Site payments and processes as needed.
    • Schedule and/or perform study procedures as per study requirements and delegation of responsibilities.
    • Prepare for and participate in onsite study audits or regulatory agency inspections.

     

    • A university degree in Life Science, preferably in pharmacy, nursing or lab analytics.
    • Minimum of 2 years of on-the-job experience as a site coordinator
    • Ability to work in a fast-paced environment, with short timelines and multiple tasks to be completed simultaneously.
    • Ability to effectively communicate in stressful situations and demonstrate the ability to problem-solve in an effective and efficient manner.
    • Flexibility in working hours may be required depending on the schedule of study procedures and/or patient visits.
    • Fluent English and Local Language

    If you feel it is time to make your skills and knowledge visible within a developing company with true focus on its people, then Milestone One is the right choice for you.

    About this role

    Summary

    Support clinical study activities, manage site data, coordinate visits, and ensure compliance.

    Job title

    Clinical Site Coordinator

    Experience level

    2+ years

    Industry

    healthcare

    Location requirements

    Vienna, remote work allowed

    Salary

    Not specified

    Management role

    No

    Skills & keywords

    Required skills

    communicationregulatory documentationdata entryclinical trial coordination

    Preferred skills

    ICH-GCPregulatory inspectionsclinical supplies management

    Specializations

    clinical trialsregulatory documentsdata entrypatient enrollmentstudy coordination
    Locations

    Structured locations inferred from the posting.

    Vienna, Austria

    On-site City

    Vienna, Austria

    Remote City
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