Safety Specialist You will be responsible for the overall co-ordination of the serious adverse event (SAE) processes as well as the co-ordination of database activities for projects. You will maintain knowledge and understanding of PPD SOPs and WPDs; current global regulations and ICH/local guidelines regarding clinical trials, regulatory documents and safety issues; and effectively interface with project teams, client company, and investigators regarding SAE activities. The Safety Specialist is involved in the preparation and revision of department SOPs and WPDs as well as preparing for and attending audits. Candidates should have a Life Sciences degree or be a licensed health care professional. Previous experience in a pharmaceutical, clinical or healthcare setting (preferable in PVG/drug safety). This experience should ideally include experience in all stages of the PVG process and a proven understanding of all relevant ICH guidelines. WHEN YOU APPLY FOR THIS ROLE YOU WILL BE AUTOMATICALLY TRANSFERRED TO OUR WEBSITE. PLEASE USE REFERENCE NUMBER 00189 TO APPLY | 