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Clinical Trial Assistant

Posted 7 hours 47 minutes ago by Fundació Privada Món Clínic Barcelona

Permanent
Full Time
Academic Jobs
Cataluña, Barcelona, Spain
Job Description

We are a private, newly created, and non-profit Foundation, linked to the Hospital Clinic de Barcelona, whose mission is to strengthen people's health and improve the quality of life of citizens.

We're hiring a Clinical Trial Assistant to join the Barcelona Clinical Coordinating Center (BCCC), an academic Contract Research Organization (CRO) based in Barcelona. This is a great opportunity.

Responsibilities:


The incorporated person will be responsible for:


  • Assist Clinical Research Associates (CRAs) and Regulatory and Start-Up (RSU) team.
  • Collection, and archiving of site information and documents during startup.
  • Assistance in preparation of submission package to ECs/HA (initial,
  • substantial amendments) and submission to EC/CAs
  • Assist in the preparation of study and site-specific materials in accordance with relevant SOPs.
  • Assist with Clinical Trial Agreement preparation, review and signatures.
  • Preparation and maintenance of Investigator site file (ISF) and Trial Master File (TMF).
  • Assist with periodic auditing/quality review of trial documentation.
  • General administrative support to Project Manager and Coordinating monitor.
  • Coordinate the shipment and tracking of study materials (paper ISF, CRFs, lab supplies ).
  • Assist in coordinating investigator payments.

Requirements:


  • Baccalaureate, higher vocational training in administration or university degree in the sciences (preferably in life sciences, medicine, or nursing)
  • More than 1 year of experience in clinical trial administration in research (CRO, Pharma Industry, cooperative research groups, etc.)
  • Written and verbal communication skills, good command of English language
  • Computer literacy: working knowledge of Microsoft word, excel, Outlook.
  • Effective time management and organizational skills.


Valuable:


  • Knowledge of applicable regulatory requirement, GCP and ICH guidelines.
  • Knowledge of clinical database applications for eTMF and CTMS.



Working conditions:


  • Full time position
  • Offices located in the center of Barcelona
  • Competitive salary range
  • Starting: June-July 2025.
  • Benefits Club




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