Senior Clinical Research Associate

hace 3 días

Ourense, España Upsilon Global A tiempo completo

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 #J-18808-Ljbffr

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