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Alimentiv

Posted 20 days ago

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Join our Talent Pool - Sr Clinical Research Associate (Serbia)

BelgradeRemote

AI Summary

Senior Clinical Research Associate at Alimentiv, based in Belgrade, responsible for site monitoring, study management, mentoring junior CRAs, and acting as a subject matter expert across multi-centre clinical trials in Serbia and Croatia.

About this role

We are proactively inviting qualified candidates to join our talent pool for anticipated Clinical Research Associate (CRA) needs. At Alimentiv, our CRA teams play a critical role in site monitoring and study management across our global clinical trial portfolio. At this time, we're primarily seeking those with clinical monitoring experience at Senior CRA level, with the ability to cover sites across Serbia and Croatia.

What the process looks like:

  • A Talent Acquisition representative will contact selected candidates to schedule a qualifying call to learn more about your experience, and what your timeline looks like
  • We'll also share details about timelines on our side - note that this Talent Pool is not necessarily for an immediate, active role
  • We'll keep your details on file and in mind - if an active vacancy does arise which matches your seniority and logistical details, we'll reach out to get an interview scheduled with the team
  • Our Talent team is actively monitoring this pool

    • Sr Clinical Research Associate

  • Act as subject matter expert, mentor, coach and/or provide performance feedback to manager for peers
  • Assist with selection, hiring, training, and supervision of CRAs as needed. Perform co-monitoring and training visits with CRAs
  • When required, act as the first escalation point for the resolution of site/patient issues or to address Sponsor concerns
  • May represent Director, Monitoring and Site Management or Manager, Clinical Site Management in BD initiatives with a site monitoring focus
  • May be assigned Lead CRA role and manage monitoring services for a group of projects and/or CRAs on large/complex project(s) including directing/guiding day to day activities and review/approval of monitoring reports
  • Oversee overall integrity of the study to promote positive working relationships with the site and staff
  • Ensure SOPs in place to optimize patient recruitment providing guidance to site teams of inclusion/exclusion criteria

    • Qualifications

  • Applicants should have relevant clinical monitoring experience, with Senior CRA candidates expected to have several years of progressive on-site and/or remote monitoring experience across multi-centre clinical trials
  • Valid driving license may be required depending on site coverage needs

    • Compensation/Total Rewards

    Compensation may vary depending on the role seniority, geographic location, and candidate experience.
    All full-time, permanent roles will include a base salary + eligibility for performance-based bonus, as well as a variety of benefits which vary by location, but are designed to ensure you feel supported.
    If contacted for an initial call, a member of our TA team will be happy to share more.

    Skills

    Clinical MonitoringCo-monitoringHiring And Supervision Of CRAsInclusion/exclusion CriteriaMonitoring ReportsPatient RecruitmentPerformance FeedbackSite MonitoringSOPsStudy Management

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