Senior CRA I​/II - Senior Klinischer Monitor; m​/w​/d

Clinical Research Associate

This position is for experienced Clinical Research Associates with 2+ years of independent monitoring experience. You will manage clinical trial sites across Germany, ensuring studies are conducted in compliance with the protocol, ICH-GCP, applicable regulations, and company SOPs.

You'll work autonomously, partner closely with investigative sites, and collaborate with project teams to deliver high-quality, inspection-ready clinical trials.

Additional responsibilities may include supporting process improvement initiatives, mentoring activities, or project-specific tasks aligned with experience.

• Review site metrics and prioritize monitoring activities based on risk
• Conduct on-site or remote monitoring visits
• Partner with sites to resolve findings and improve processes
• Collaborate with Clinical Team Managers and project teams to keep studies on track and inspection-ready
• Complete documentation, system updates, and administrative tasks

• Bachelor's degree in a life sciences related field or equivalent qualification
• Minimum 2+ years of experience as a Clinical Research Associate / Monitor
• Valid driver's license
• Full right to work in Germany
• Fluency in German and English (C1 level) – interviews will be conducted in German

Knowledge, Skills & Abilities

• Strong clinical monitoring skills with hands-on RBM experience
• Excellent understanding and application of ICH-GCP and applicable regulations
• Solid therapeutic area knowledge and medical terminology
• Well-developed critical thinking, problem-solving, and root cause analysis skills
• Strong written and verbal communication skills with medical professionals
• High attention to detail and strong organizational skills
• Ability to work independently while contributing effectively to cross-functional teams
• Flexibility and adaptability in a dynamic project environment
• Proficiency in Microsoft Office and ability to learn clinical systems (e.g., CTMS)

Locations:
Home-based or hybrid anywhere in Germany FTE:
Full-time (40 hrs/week) or Part-time 80% (32 hrs/week)

Contract:

Permanent Travel:
Approximately 50–75% (study-dependent)

Severely disabled applicants with the same aptitude will be given preferential treatment. Schwerbehinderte Bewerberinnen und Bewerber werden bei gleicher Eignung bevorzugt berücksichtigt.