GCP Auditor

CDI

Remote

Lublin, Polska

We are seeking a motivated and detail-oriented GCP Auditor to join our team in the biotechnology sector. As a GCP Auditor, you will play a crucial role in ensuring compliance with Good Clinical Practice (GCP) regulations and guidelines. Your responsibilities will include conducting audits of clinical trial sites, reviewing documentation, and ensuring that all processes adhere to regulatory standards. You will work closely with various stakeholders to identify areas for improvement and ensure that our clinical trials are conducted ethically and efficiently.

The ideal candidate will have a strong understanding of biotechnology principles and a passion for quality assurance in clinical research. You will be expected to analyze data, prepare audit reports, and communicate findings effectively. This is an excellent opportunity for fresh graduates looking to start their career in the biotechnological field.

We are looking for a fresh graduate with a background in biotechnology or a related field. The ideal candidate should possess strong analytical skills and a keen eye for detail. Familiarity with GCP regulations and experience in clinical research is a plus, but not mandatory. You should be proficient in French, as this will be essential for communication with our partners and stakeholders.

If you are passionate about ensuring the integrity of clinical trials and are eager to learn and grow in a dynamic environment, we encourage you to apply. Join us in making a difference in the biotechnology industry!

Apply now and take the first step towards an exciting career as a GCP Auditor!