The Data Manager position is responsible for contributing to the management of data used for C-Path research purposes and supporting the development of clinical/preclinical data standards. This position supports all C-Path consortia that utilize clinical and preclinical data in their projects. Position will utilize vendor and internally developed tools to identify and solve data process flow, data review and data quality problems, and to create data sub-sets required by research plans. Position will also assist with the design and implementation of logical and physical databases. Continue reading
The Critical Path Institute, a non-profit organization headquartered in Tucson, Arizona, invites applications from Master’s level (PhD preferred) scientists with expertise in genetic data analysis and processing to work collaboratively as a guest researcher with the Centers for Disease Control and Prevention, Division of Tuberculosis (TB) Elimination, Laboratory Branch in Atlanta.Continue reading
The Assistant/Associate Director is responsible for assisting the Executive Director in the overall management of the PRO Consortium to include advancing and documenting the science of clinical outcome assessment (COA) endpoint development and testing for use in clinical trials designed to evaluate the safety and efficacy of new medical products. In addition, the Assistant/Associate Director is responsible for directing the scientific and operational activities of the Electronic Patient-Reported Outcome (ePRO) Consortium. Continue reading
Critical Path Institute is a large multi-disciplinary scientific non-profit organization focused on accelerating the development of new therapies. CAMD is dedicated to Alzheimer’s and Parkinson’s disease. The Senior Project Manager works in close partnership with the CAMD Executive Director to provide operational and project management excellence for C-Path and affiliates’ virtual working groups to advance drug development tools and therapies to treat brain diseases. Additionally, the Sr. Project Manager will be responsible for ensuring that the Parkinson’s team meets the requirements of the grants which fund this work.Continue reading
Learn how AZBio Purchasing Programs to help your dollars take you farther.Continue reading
Pinnacle Transplant is currently seeking a Research and Development Senior Manager. Continue reading
TGen’s paid summer internship program in biomedical research – Helios Scholars at TGen – is now accepting applications through Feb. 13. Continue reading
National Cancer Institute: Building on Opportunities in Cancer Research 2016 describes current opportunities to build on and advance cancer research.Continue reading
|Job Title: AA||Microbiology Applications Engineer||Job Status: exempt||Full Time / Exempt|
|General Description: Work based in Tucson, AZ|
|To serve as a bridge between product development and sales by developing, supporting and representing the Company’s technology in an industrial environment, through use of knowledge of engineering and programming as well as sophisticated instruments and computers.
To identify customer best fit with Company’s product & assist in development of technical documents and training programs, maintaining customer cGMP compliance. To work independently and as a team player on simultaneous projects with compressed timelines; traveling up to 50% of the time interfacing with customers and attending or exhibiting at conferences and trade shows.
|Product development engineering support for both hardware and software technologies to support real time microbial detection and analysis.
|BA/BS or MS in biological discipline with at least two years work-related experience. Practical experience in industrial/R&D lab environment with focus toward microbiology. Experience with laboratory instrumentation, technology and tools. Self-motivated with a strong work ethic; independently or as part of a team. Strong written and oral communication skills. Good computer skills; minimum of Word, Excel, Power Point with NI LabView experience preferred. Knowledge of or experience with cGLP or cGMP environment. Competitive salary and benefits commensurate with experience.
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