Study Monitor Support Specialist

• Support NonClinical Toxicology Study Monitors with key study activities
• Support of external study monitors by supporting key support activities
• Maintain and update supporting documents
• Support the identification and implementation of effective toxicology study processes within the study monitor group that improves efficiency and simplifies ways of working. Provide continued evaluation of the end-to-end process for CRO study management to identify weaknesses and gaps with a focus on improving and simplifying wherever possible.
• Support financial aspects of study conduct (approval and review of Amended Statements O f W ork / Invoice s / Purchase orders)
• Maintain tracker for ongoing study costs
• Support ad hoc request for metrics and information gathering activities
• QC check of submission documents

Essential Skills/Experience:

• Fluent in English (spoken and written)
• Strong candidates will have some experience of working in a GLP Toxicology lab and understand the practices, principles and concepts associated with planning and delivering a fit for purpose non-clinical toxicology stud y
• Ideally BS c in Pharmacology / Toxicology.
• Experience of delivery to multiple concurrent projects .
• Strong stakeholder management skills with excellent communication skills
• Experience in improvement projects with a drive to ensure ways of working are efficient.
• A dedicated team player with excellent communication and influencing skills with experience working in multidisciplinary matrix teams across a broad spectrum of geographical locations .
• Results orientated with high scientific standards to support project execution.
• Proficient in the use of Microsoft Office products