Clinical Development Manager
To design, coordinate, and provide oversight of clinical trials sponsored by Chimerix. Develop, write, and/or coordinate generation of clinical study documents including, but not limited to, clinical trial protocols, Investigator Brochures, clinical sections of regulatory submissions, and clinical study reports. Provide scientific expertise and leadership on assigned compounds to investigators, collaborators, vendors, and other key personnel. Please send resumes to hr@chimerix.com
Director, Quality Assurance (QA)
To direct and manage Chimerix's Quality Assurance program. Responsible for establishing and managing all Quality Assurance projects. Creating, implementing and maintaining corporate-wide Quality Assurance systems and Quality Assurance strategies for all GMP, GCP, and GLP activiites. Develop, direct and manage GMP, GLP and GCP audit programs. Please send resumes to hr@chimerix.com
Improve human health by developing important new antiviral medicines to treat life-threatening diseases.
Chimerix was founded with the aim of radically improving the way viruses are treated. We initially saw an opportunity to combine a known antiviral with an intriguing technology to create a new treatment option for smallpox, historically one of the greatest viral threats to humankind. As we learned more about CMX001, we have seen its potential across numerous applications. Read More