DSRD Study Enabling & Execution is a global group composed of subject matter experts in study and project execution, training, compliance and systems, who plays a critical role in the success of DSRD. As a highly valued partner, we focus on the development, empowerment, and leadership of our colleagues to ensure their growth and success. The In Vivo Technician role functions within study execution and provides non-GLP and GLP in vivo study conduct expertise to advance the Pfizer portfolio, particularly for the selection of new therapeutic candidates but also for support of later stages of clinical development and registration. The In Vivo Technician is responsible for performing accurate, high quality in-life study work for rodent and non-rodent safety studies in compliance with the study protocol, Standard Operating Procedures (SOPs), Good Laboratory Practice (GLP) regulations, Environmental Health and Safety (EHS) standards, animal welfare regulations, and departmental policies/procedures. The data collected on these studies by the In Vivo Technician enable candidate selection, first-in-human studies, 13-week or longer studies and early research and target safety and investigative work.