A leading global provider of clinical research services is seeking a candidate in Reading to coordinate and support the uploading of CPP documents while ensuring compliance with global procedures. Responsibilities include preparing and reviewing scientific documents, implementing quality control processes, and collaborating with cross-functional teams. A Bachelor’s degree in health sciences or related field is required, alongside industry experience in scientific writing and document quality assurance. The role offers an opportunity to contribute to innovative medical treatments. #J-18808-Ljbffr