Clinical Research Associate – Remote/Travel (Germany)

Allucent; Amsterdam; Hybrid; EUR 42,000 - 65,000; Full time

Benefits offered by this job

Comprehensive benefits package

Flexible working hours

Remote/office‑based options

Training budget

Buddy Program

Career progression

Job summary

Allucent™ is seeking a Clinical Research Associate (CRA) to join the A-team. You will independently monitor investigational sites, pro‑actively detect issues, and ensure clinical studies are performed according to the trial protocol and in compliance with SOPs, applicable regulations, and the principles of Good Clinical Practice.

You will take the lead on monitoring activities, owning sites and relationships with investigators.

Qualifications

• Experience leading monitoring activities in complex trials (minimum 2 years).
• Strong understanding of ICH‑GCP and regulatory guidelines.
• Clear and confident communicator in English and German.
• Willingness to travel, as required (8 DOS per month).

Responsibilities

• Independently manage monitoring for assigned clinical trials across study phases, including site initiation, routine monitoring, and close‑out visits.
• Ensure compliance with protocols, GCP, ICH, SOPs, and applicable regulatory requirements.
• Build strong site relationships, acting as a primary contact and ensuring high‑quality data collection.
• Identify and resolve site issues, escalating as needed to maintain trial integrity and patient safety.
• Activities around regulatory affairs, site activation and study‑startup.

Skills

Monitoring

Regulatory knowledge

Communication English+German

Travel readiness

Job description

Allucent™ is seeking a Clinical Research Associate (CRA) to join the A-team. You will independently monitor investigational sites, pro‑actively detect issues, and ensure clinical studies are performed according to the trial protocol and in compliance with SOPs, applicable regulations, and the principles of Good Clinical Practice.

You will take the lead on monitoring activities, owning sites and relationships with investigators.