Clinical Trial Assistant

Clinical Trial Associate (CTA) - 6-Month Contract

Remote (EU-based) or On-site in Barcelona

Full-Time Contract via Oxford Global Resources

Start date: Early May 2025

Oxford Global Resources is partnering with Leading Biotech Company, a global leader in molecular diagnostics and sample-to-insight solutions, to support an exciting 6-month contract opportunity for an experienced Clinical Trial Associate (CTA).

We're looking for a proactive and detail-oriented CTA to contribute to multiple clinical studies. You'll play a key role in document and trial management, with a strong focus on eTMF oversight (Veeva Vault) and IVD study support.

Key Responsibilities

• Maintain Trial Master File (eTMF) in Veeva Vault, ensuring inspection readiness.
• Assist in study start-up, maintenance, and close-out activities across global studies.
• Support tracking of regulatory documents, site communications, and essential trial documentation.
• Collaborate closely with Clinical Project Managers, CRAs, and internal stakeholders.
• Support cross-functional teams to ensure timelines and quality metrics are met.

What We're Looking For

• Previous experience working as a CTA in clinical research settings.
• Hands-on experience with Veeva Vault eTMF is essential.
• IVD experience highly preferred; CDx is a plus but not required.
• Strong organizational and communication skills.
• Ability to work independently in a remote setup or hybrid from the Barcelona office.
• Fluent in English.

Details

• Duration: 6 months
• Hours: 40 hours/week
• Start date: Early May 2025
• Location: Remote (within the EU) or based in Barcelona

If you are passionate about clinical research and ready for your next challenge in a dynamic international environment, we'd love to hear from you!

Apply now or reach out to Susagna Sastre at Oxford Global Resources for more information: