Freelance CRA

PSI CRO · Other US Location

Company

PSI CRO

Location

Other US Location

Type

Full Time

Job Description

Company 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.

    Job Description

    We are looking for experienced clinical trials monitoring professionals to support us with new sites activation, identification, and on-site trial coordinating.Ā 

    Your tasks:

    • ActĀ as the main line of communication between the Sponsor or CRO and the site.
    • EnsureĀ response to feasibility questions are provided in due time.
    • AssistĀ in scheduling and preparation for all types of monitoring visits at the medical institution/research center.
    • Be present and available to respond to monitors duringĀ all types of monitoring visits conducted at the medical institution.
    • TrackĀ patient enrollment and actively supportĀ the medical site and CRO/Sponsor team in meeting project timelines and enrollment goals.
    • MaintainĀ 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, handleĀ and maintainĀ all site-specific regulatory documents as needed.
    • FacilitateĀ and support the contract and budget negotiations at the site level.
    • SupportĀ Investigator and Site payments and processes as needed.
    • ScheduleĀ and/or performĀ study procedures as per study requirements and delegation of responsibilities.
    • PrepareĀ for and participateĀ in onsite study audits or regulatory agency inspections.

    Qualifications

    • A university degree in Life Science, preferably in pharmacy, nursing or lab analytics.
    • Minimum of 2 years of on-the-job experience in a clinical trial environment, as a Study Coordinator or similar function.
    • 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.
    • Valid US Driver's License with the ability to travel as needed.
    • Flexibility in working hours may be required depending on the schedule of study procedures and/or patient visits.

    Additional Information

    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.

    Apply Now

    Date Posted

    01/24/2025

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