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