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Trial Committee Specialist (Clinical Trials) - Hybrid in Belgrade

syneoshealth · SRB-Belgrade-Hybrid

Nouveau
Hybrid Mid 🇬🇧 English
Microsoft Office Good Clinical Practice (GCP) Trial Master File (TMF)

Description du poste

About the role

Syneos Health is hiring a Trial Committee Specialist for a hybrid position in Belgrade, Serbia. The role covers the end-to-end setup and operation of clinical trial committees, from identifying members and managing contracts to running meetings, reviewing clinical data and supporting the Committee Manager.

Key responsibilities

  • Identify potential members for trial committees and collect and assess their documents (e.g. NDAs, CVs), including debarment checks and conflict of interest attestations.
  • Negotiate and execute contractual agreements, and track committee member invoices against the project budget.
  • Follow the Committee Charter and project plans: schedule and attend meetings, prepare and distribute agendas, minutes and action items, and distribute safety listings, expedited safety reports and protocols.
  • Review clinical event and endpoint documentation for completeness, redact protected health information and flag unreported events, then initiate queries to sites and follow them to resolution.
  • Manage translation services, including submission, tracking and assurance of page equivalents.
  • Support User Acceptance Testing of the committee's collaborative workspace or electronic adjudication platform.
  • Provide operational support to the Committee Manager on metric reporting and file all trial committee documents in the Trial Master File (TMF).

Required profile

  • Bachelor's degree in Life Sciences, Medicine, Pharmacy, Nursing or a related field, or an equivalent combination of education and experience.
  • Previous experience in study coordination or within a CRO, pharmaceutical or biotechnology company preferred.
  • High level of written and spoken English; willingness to travel approximately 5% preferred.

Required skills

  • Knowledge of Good Clinical Practice (GCP) and ICH guidelines, and other applicable regulatory requirements.
  • Proficiency in Microsoft Office.
  • Strong organizational and time management skills, attention to detail and excellent communication skills.

Questions fréquentes

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Source : ats:workday

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syneoshealth

SRB-Belgrade-Hybrid