Clinical Research Associate I, Klinischer Monitor

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

📋 Description

• Executes and oversees all facets of the clinical monitoring and site management processes.

• Performs remote or on-site visits to evaluate compliance with protocols and regulations while managing necessary documentation.

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

• Guarantees readiness for audits.

• Fosters collaborative relationships with investigational sites.

• Implements a risk-based approach to monitor investigator sites.

• Evaluates investigational products through physical inventory and record assessments.

• Shares accountability with other project team members in resolving issues and findings.

⛳️ Requirements

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

• Prior experience in a clinical setting with exposure to clinical research, healthcare, or clinical trials.

• Valid driver's license.

• Full right to work in Germany.

• Proficiency in English and German at a minimum C1 level.

🏝️ Benefits

• Competitive salary.

• Opportunities for professional development.

• Flexible work arrangements.