Clinical Research Associate

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

📋 Description

• Oversee and take responsibility for the advancement of clinical studies at investigative sites.

• Ensure that clinical studies are carried out, documented, and reported in compliance with the protocol, SOPs, ICH-GCP, and relevant regulations and standards.

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

• Identify and select investigators for the studies.

• Assist in the preparation of regulatory submissions.

• Conduct pre-study and initiation visits to ensure readiness.

• Concentrate on an average of one to two studies and develop expertise in the associated protocols.

• Recognize potential risks associated with studies and suggest appropriate mitigation strategies.

⛳️ Requirements

• A graduate or postgraduate degree in a scientific or healthcare field.

• A minimum of one year of experience as a Clinical Research Associate (CRA) in a Contract Research Organization (CRO) or within the pharmaceutical/biotech sector, or equivalent relevant experience and/or demonstrated competencies.

• Experience in site management or a similar role within clinical research.

• Outstanding communication and organizational abilities.

• Ability to work effectively as part of a team.

• Proven client-focused approach.

• Willingness to travel domestically, including overnight stays, approximately 50–60% of the time; some senior roles may require international travel.

• Proficiency in both English and German.

• Experience in oncology, CAR-T, or First-In-Human (FIH) studies (phase III).

🏝️ Benefits

• Reasonable travel requirements and enhanced work/life balance.

• Support from direct line management.

• Opportunity to make an impact in a smaller CRO environment.

• Employee contributions and ideas are appreciated and encouraged.