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

📋 Description

• Oversee and take ownership of the progress of clinical trials at investigative sites.

• Ensure that clinical trials are performed, documented, and reported in accordance with the protocol, SOPs, ICH-GCP, relevant regulations, and standards.

• Organize the activities necessary for the setup and monitoring of studies.

• Identify and select investigators.

• Assist in the preparation of regulatory submissions.

• Conduct pre-study and initiation visits.

• Provide insights and drive positive changes within the organization.

⛳️ Requirements

• Bachelor’s or Master’s degree in a scientific or healthcare-related field.

• Minimum of one year of experience as a CRA in a CRO or the pharmaceutical/biotech industry, or equivalent relevant experience and/or demonstrated competencies.

• Experience in site management or an equivalent role in clinical research.

• Strong communication and organizational abilities.

• Collaborative team-oriented mindset.

• Demonstrated client-focused approach.

• Willingness to travel domestically, including overnight stays, up to approximately 50–60%; international travel may be necessary for certain senior roles.

• Proficiency in both English and German.

• Experience in oncology, CAR-T, or first-in-human (FIH) studies (phase III).