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.

#J-18808-Ljbffr

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