ARO Platform offers a complete package to Sponsor for
managing the necessary activities, from start to finish, for
conducting trials (from phase I to phase IV) and clinical studies.
VHIR offers a vacant position within its ARO for a Clinical Project
Officer to develop and manage activities in Clinical Trials. Main
responsibilities and duties: Provide scientific and methodological
guidance to project coordinators and sponsors to assess and ensure
the feasibility and robustness of clinical research projects
Provide strategic regulatory support and guidance to investigators
throughout the planning and execution of clinical research
projects. Manage and oversee the preparation, adaptation, and
submission of all regulatory documentation required for project
approval by relevant authorities Act as the primary point of
contact for investigators/sponsor, ensuring continuous support
throughout the full project lifecycle, including documentation
management and issue resolution. Coordinate and manage
communication with all stakeholders involved in project execution,
including external vendors and service providers. Lead and
coordinate the activities of Clinical Research Associates (CRAs)
and Clinical Trial Administrators (CTAs) assigned to each project,
ensuring alignment with project timelines and objectives. Supervise
study start-up, monitoring, and close-out activities, including the
review and approval of corresponding reports. Ensure that all
project activities are conducted in compliance with applicable
regulations, Good Clinical Practice (GCP), and the unit’s quality
management system, while actively promoting continuous process
improvement. Support additional project-related tasks and
cross-functional initiatives as assigned by management. Education
and qualifications: Required: Degree or equivalent in Health
Sciences Training in monitoring clinical trials. Fluency in
Catalan, Spanish and English (professional proficiency) Desirable:
Additional or specialised training