What we’re looking for:
As a Study Data Manager (SDM) you will perform Data Management activities that support Sinclair’s pre-clinical projects within the Data Acquisition System (DAS) mainframe. You’ll be an active member of a multi-disciplinary team to plan and execute the Data Management tasks required for regulatory toxicology studies under the FDA SEND requirements. You will ensure that the employees are collecting and recording raw data and performing the study according to protocols, Standard Operating Procedures (SOPs) and GLP requirements. You may even assist in data collection and study procedures yourself!
What you’ll need:
A Bachelor degree in Animal Science or related field with a minimum of seven years of experience within the pre-clinical research field is preferred or an equivalent combination of education and experience within a related setting.