Senior Clinical Research Associate

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.

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 applications@upsilonglobal.com