Cellix Bio employees and teams apply sound science to develop and deliver medicines that focus on unmet medical needs around the world. Our current prescription products at various stages of development target to serve patients across therapeutic areas including metabolism, immunology, infectious diseases, neuroscience, ophthalmology, and oncology. Here, everyone matters and you will be a vital contributor to our inspiring, bold mission. You will help make an impact on people\xe2\x80\x99s lives and change futures every day. We are equally committed to bringing out your best and fostering a collaborative workplace built on trust and respect. We empower our people to take charge of their potential. We offer training and leadership development programs tailored to help you build valuable skills and succeed in your career. As you discover your potential, your professional and personal future will become brighter. Forward your CV / Resume : careers@cellixbio.com

SENIOR MANAGER, Pre-Clinical To direct investigative safety studies that support de-risking of innovative drug targets and modalities, non-clinical compound candidate selection. Develop strategy for bringing in state of the art techniques, and apply them to prospective and retrospective in vivo, ex vivo and in vitro evaluations of drug safety, with a particular emphasis on comparative biology of innovative therapeutic targets, pathways and modalities. Nonclinical investigative safety assessment plan to support development/registration of drugs of various and novel modalities. PhD in pharmacology, toxicology, immunology, molecular biology, biochemistry, cell biology or a related biological science; MD, DVM, PharmD with at least 5 years of experience in the related field. Demonstrated leadership in cross-industry organization. An understanding of the drug development process and how investigative science plays a role in quickly and efficiently addressing key questions.