Upsilon Global are seeking a freelance SCRA based in the Galicia region of NW Spain to support an ongoing study into a respiratory virus. This is an ongoing study linked to 1-2 key sites in the region, with local Galician language being essential for the ICFs.
Para presentar una candidatura, simplemente lea la siguiente descripción del puesto y asegúrese de adjuntar los documentos pertinentes.
This is an immediate start for 0.4 FTE on an initial 6‑month contract.
Key information:
* Position: Freelance SCRA
* Employment: Freelance
* FTE: 0.4FTE
* Indication: Respiratory Viruses
* Start Date: January 2026
* Travel: Minimal, Galicia region
* Location: Galicia, NW Spain
Key Responsibilities:
* Conduct on-site visits, monitoring and assessment of clinical trial site, ensuring adherence to study protocols, Good Clinical Practice (GCP) guidelines, and applicable regulatory requirements.
* Perform source document verification, data collection, and accurate recording of study data, ensuring data integrity and compliance.
* Collaborate with site investigators, site staff, and study team members to ensure successful execution of clinical trials.
* Assist in the development and review of study documents, including protocols, informed consent forms, and case report forms.
* Maintain effective communication with study site, sponsors, and other stakeholders to provide timely updates, address queries, and resolve issues.
* Monitor subject safety, reporting adverse events, and ensuring appropriate follow-up actions are taken.
* Contribute to the preparation and coordination of study initiation, monitoring, and close‑out activities.
* Assist in the preparation and participation in regulatory inspections and audits as necessary.
* Stay updated with current regulations, guidelines, and industry trends related to clinical research in translational/early‑phase trials
Experience:
* 5+ years independent monitoring experience
* Experience in respiratory viruses preferred
* Fluency in written and spoken Galician essential
* A strong background in early‑phase / phase I/II trials
* In-depth knowledge of local regulatory requirements and clinical trial processes.
* Strong organizational and communication skills, with the ability to manage multiple priorities.
* Ability to work independently, demonstrating initiative, attention to detail, and problem‑solving skills
For more information, please apply via the link or contact
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