It’s not news that the number and complexity of clinical research studies continues to grow as the workforce continues to dwindle. Consequently, sites are continually being asked to do more.
While demand for skilled clinical research professionals is at an all-time high, identifying candidates with the required skill sets is challenging.
This blog identifies applicable regulations and outlines regulated documents and data in clinical research and the systems used by sponsors, contract research organizations (CROs), monitors, and research sites to collect, exchange, and store them.
All clinical researcher professionals receive extensive training on Good Clinical Practice and other processes to be followed in their work. A topic that is only superficially covered is why those processes are required.
Get into the 2022 holiday spirit with these hand-picked tunes—both old and new—from the staff at ACRP. No matter if you're resolutely committed to the Christmas classics that have been […]