The CRN II works with the PI, department, sponsor, and institution to support and provide guidance on the administration of the GCP compliance, financial and other related aspects of the research study.
Maintain transgenic mouse colony, including breeding, weaning, ear tagging, genotyping, cells injections, drug administration, blood and other fluid collection, prepare IACUC reports and protocol amendments, ensure compliance with IACUC regulations.
Assist with collection of supporting documentation for contract packages , IACUC/IRB protocols for projects performed under this contract, research proposals and protocols, manuscripts, research SOPs, reports and presentation editing/review. Assists in initiating and maintaining regulatory IACUC/IRB requirements.
Provide supervision and guidance to junior scientist contract personnel in writing protocol-driven research proposals, animal use protocols, human use protocols, technical reports, final reports, and peer-reviewed manuscripts.
The candidates are expected to apply silicon microfabrication technology, integrated with laboratory techniques such as electrochemistry, to fabricate nanomaterials and nanodevices for biomedical applications, and further develop standard procedure towards cGMP manufacture towards clinical translation.
Calculates molarity and accurately prepares media solutions and reagents, using pH meter, balances, flow cytometry, electrophoresis apparatus, the use of acids and polyacrylamide solutions, flammable materials and other biohazards according to OSHA and institutional safety policies.
Develops and manages independent grant portfolio; Designs, develops, or adapts equipment used in experiments or research to obtain desired results;Performs and supervises those procedures which require a highly developed technical skill.
Reviewing and interpreting environmental permits and air permit applications. Preparing and performing QA/QC and technical review of emissions inventories, air quality, greenhouse gas, and air modeling calculations.
This position performs all routine and complicated laboratory procedures including specimen processing and handling, testing of patient specimens, calculating and reporting of results, performance of quality control procedures, operation and maintenance of instruments and equipment, assisting in the development of new procedures and protocols, may perform phlebotomy and other patient oriented tasks, and may perform other related duties as requested or directed.
This role will be responsible for hypothesis development, data acquisition, model development and visualization in support of data driven decisions. You will work closely with AMD's R&D, Supply Chain and IT functions.