CRA I/II – Klinischer Monitor

This is a fully remote position, open to applicants in Germany.

📋 Description

• Manages and coordinates all facets of the clinical monitoring and site management process.

• Executes remote or in-person visits to evaluate adherence to protocols and regulations, while overseeing necessary documentation.

• Serves as a specialist in site processes, ensuring that the trial is executed in line with the approved protocol, ICH-GCP guidelines, relevant regulations, and SOPs.

• Guarantees readiness for audits.

• Fosters cooperative relationships with investigational sites.

• Oversees investigator sites using a risk-based monitoring strategy, employing root cause analysis, critical thinking, and problem-solving skills to pinpoint failures in site processes.

⛳️ Requirements

• Bachelor’s degree in a life sciences-related discipline or an equivalent and relevant formal academic/vocational qualification.

• Prior experience that equips the candidate with the knowledge, skills, and abilities necessary to fulfill the role.

• Valid driver’s license.

• Full right to work in Germany.

• Fluency in English and German at a minimum of C1 level.

🏝️ Benefits

• Health insurance.

• 401(k) matching.

• Flexible working hours.

• Paid time off.

• Opportunities for professional development.