Job Description


Clinical Safety Scientist

DescriptionProcessing, follow-up and expedited reporting of spontaneous case reports of adverse events and pregnancies.Answering telephone inquiries from healthcare professionals relating to adverse event case reports. Input of data to in-house safety database.Liaison with medical personnel in GSK regarding adverse event reports.Administrative activities relating to case processing, for self and on behalf of Clinical Safety Group.Assistance with International Spontaneous Reports Group activities as required and authorized by line manager.Researching new raw data ae terms, mapping of raw data ae terms to dictionary codes and coding conventions.Additional information about the processAll profiles will be reviewed against the required skills and experience. Due to the high number of applications, we will only be able to respond to successful applicants in the first instance. We thank you for your interest and the time taken to apply