Clinical Trial Associate

☞ Hobson Prior

View: 165

Update day: 04-11-2025

Location: Charleroi Hainaut

Category: Administrative / Clerical / Assistant Science Consulting / Customer Service

Industry: Biotechnology Research

Position: Associate

Job type: Contract

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Job content

Hobson Prior is seeking a Fulltime Clinical Trial Associate with a strong background in clinical trials. This role will working with a growing Biotech to assist the Project Managers in clinical oncology studies. The successful candidate will participate in all phases of clinical studies including start up, study maintenance, and close-out activities in addition to performing additional day to day activities under the guidance of the Sr. CTA/Lead, Assistant Project Managers and Project Managers and liaise between field and office and are expected to work more autonomously and independently than the CTA

Job overview:

  • In this position, you will be responsible for overseeing document management, monitoring, assessment, and archival of trial master files
  • Ensure study documentation, communication, training and data collection is aligned with study protocol adherence, and all applicable SOPs, regulations and guidelines.
  • Contribute to the selection, establishment, and supervision of our vendors, which may include CROs, central labs, clinical study supply services, and electronic data capture (EDC) providers
  • Aid in the creation, implementation, and maintenance of our quality management system (QMS) and procedures
  • QC Trial Master File (for clinical projects where individual is not setting up and maintaining the file).
  • Collaborate with both internal and external teams to ensure all study-related activities adhere to company SOPs, ICH GCP, and UK regulatory requirements
  • Assist in site budget and contract negotiations, as well as the creation and review of vital documents such as protocols, patient information sheets, consent forms, case report forms, study plans, and clinical study reports
  • Undertake any other assigned responsibilities

Requirements:

  • Previous experience in a CTA, trial coordinator, or research nurse role would be advantageous
  • Proficiency in relevant clinical research regulatory requirements, including GCP
  • Familiarity with essential management within a TMF would be beneficial
  • Strong interpersonal and written communication skills
  • Oncology experience is preferred
  • English speaking
  • Happy with Travel to the site 2-3 times a week
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Deadline: 19-12-2025

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