We support research sites at every stage – from the first organizational steps to conducting clinical trials in accordance with international standards.
Branża badań klinicznych mierzy się dziś z niedoborem doświadczonych koordynatorów oraz wysoką rotacją na stanowiskach operacyjnych.
Dlatego stworzyliśmy program stażowo-rozwojowy, który:
łączy ośrodki badań klinicznych z wstępnie przeszkolonymi kandydatami,
umożliwia bezpieczne wdrażanie nowych osób bez kosztów rekrutacyjnych,
daje ośrodkom realny wpływ na jakość przyszłych kadr.
👉 Pobierz PDF i poznaj szczegóły programu współpracy
We support research sites in searching for and implementing the personnel necessary for the proper functioning of the research team. We help in creating job descriptions, recruitment, and provide introductory training so that each employee can quickly start working in accordance with the requirements.
We prepare a complete set of Standard Operating Procedures (SOPs) and internal documentation that meet the requirements of sponsors and inspections. This ensures that the site operates in an organized manner, in compliance with regulations, and is ready for audits.
We create professional informational materials about the research site – from presentations to sponsor packages. Thanks to them, the site gains credibility, and sponsors can make collaboration decisions more quickly.
We provide training for research teams, including the “ICH GCP E6(R3)” course, completed with a certificate accepted by TransCelerate. This ensures that the staff works in accordance with international standards of quality and ethics.
We do not leave the site on its own after implementation – we offer ongoing advisory support. We are available whenever questions, doubts, or the need to adjust procedures to the requirements of new clinical trials arise.
Research sites have trusted us, and thanks to our support, they have started their operations and launched their first clinical trials.
