I’m partnering with a clinical-stage biotech to find experienced CRAs in SPAIN and GERMANY to support their ongoing clinical development programmes. Respiratory trial experience is a strong plus, but CRAs from adjacent therapeutic areas with transferable monitoring experience are very welcome to apply. Remote, field-based with regular site travel Germany: 0.4 FTE, increasing to 1.0 FTE in the new year The role

Independently manage your own portfolio of investigational sites Conduct qualification, initiation, routine monitoring and close-out visits in line with ICH-GCP Carry out SDV and protocol compliance checks, and **escalate** deviations and risks Act as the main point of contact for investigators and site staff Work closely with CTMs, CPMs and cross-functional study teams What we’re looking for





Proven experience as a CRA in a pharma, biotech or CRO setting A track record of independent on-site monitoring across the full study lifecycle Strong working knowledge of ICH-GCP Comfort juggling multiple sites and competing priorities Based in Spain or Germany, with fluent local language skills Flexibility to travel regularly to sites Nice to have

Respiratory or adjacent TA experience Sponsor-side monitoring experience Experience on complex, multicentre trials If you’re a hands-on CRA who enjoys owning site relationships and working with minimal supervision, I’d love to hear from you.

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📌 Contract Clinical Research Associate (Málaga)
🏢 Hlx Life Sciences
📍 Málaga