All resumes should be sent to careers@tapimmune.com
Employment Opportunities
Project Manager Experienced biotechnology project manager with knowledge of clinical operations, outsource contracting, project planning and oversight.
Director of Virology Expertise in the design and construction of novel viral expression systems, experience with molecular engineering of vaccinia virus and adenovirus a plus. Analytical methods development for both in vitro and in vivo measures of expression efficacy. Candidate is expected to develop a portfolio of expression constructs targeting viral diseases, and to explore external collaborations and grant opportunities. Special emphasis given to the areas of bio-defense and emerging infectious threats.
Virology Technician II/III (2 positions) Experience working with viral expression systems, cell culture, viral production and purification.
Scientist Molecular Immunology methods for analysis of T cell activation and function, FACS assay method development, intracellular T cell cytokine assays, Killer T cell functional methods, HLA presentation/recognition. Experience with murine tumor models and immunotherapy a plus.
Immunology Technician II/III (2 positions) Experience with cytokine assays, CTL assay methods including Cr51 release assays, FACS methods.
Analytical methods development, Scientist I. Analytical methods development in support of early stage preclinical and clinical programs. Methods for analysis of viral purity, expression of viral constructs and stability indicating methods for same.
Clinical and Regulatory Affairs manager Comprehensive knowledge of clinical and regulatory affairs, FDA guidance, IND process, CMC requirements. Reporting to the VP of development.
Document Specialist Extensive knowledge of FDA guidance regarding document systems and complicance. Experience with technical writing, document formatting and document control. Candidate is expected to establish appropriate document systems, including designs and controls for a clinical stage biotechnology company. Reporting to the manager of clinical and regulatory affairs.