Clinical Trials Assistant 1 (m/w/d), office based in Frankfurt

Yes for clinicians or healthcare graduates trying to break into the CRO industry — CTA 1 is one of the most accessible doors into clinical research. However, the posting contains no duties or pay details, so request the full description and confirm it is not purely data-entry before committing, especially given the on-site Frankfurt requirement.

Healthcare graduates, IMGs awaiting licensure or recognition, junior nurses, and pharmacists or doctors in Germany who want to enter the CRO/clinical research industry from the ground up and can work on-site in Frankfurt. Less suitable for senior clinicians seeking strategic or high-compensation roles.

Foreground protocol familiarity, documentation accuracy and regulated-record discipline drawn from real clinical work: patient record keeping, adverse event or incident reporting, SOP and guideline compliance, data capture in clinical systems, and coordination between multiple stakeholders. Add any exposure to audits, quality checks, study participation, Good Clinical Practice training or research projects, and state German and English working proficiency plus on-site availability in Frankfurt. Do not claim GCP certification or trial experience you do not have.