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 (Comunidad de Madrid)
🏢 Hlx Life Sciences
📍 Comunidad de Madrid