Plan, coordinate, and document project related activities of large scale and highly visible projects that will vary in scope and affected business units, manage resources within assigned project teams in a matrix environment, and document the project's activities.
As such the ideal candidate will be intimately familiar with machine learning, sequencing technologies and have a working knowledge of molecular biology. Design and analysis of loss and gain of function experiments to validate model predictions.
The successful candidate will join a team of investigators in using a variety of in vivo and in vitro models, to determine the cause of susceptibility to disease, and assess novel vaccine strategies and host-directed therapies that could be deployed against the disease.
Perform a variety of laboratory experiments using both routine and special techniques and methods.
Assist in more complex laboratory tasks. Record results, organize data, and perform basic computations.
Perform policy and data analyses of complex health care and human services topics and issues, which will typically require an understanding of the project's goals, the policy context, and the ability to combine and synthesize data and information from multiple sources.
Design and carry out experiments to explore the molecular mechanisms through which various signaling pathways mediated by MAPKs, Casein kinases, cell metabolism, and ER stress control bone development and remodeling.
The Residency Program Coordinator II is responsible for the coordination of a wide range of diverse administrative functions for one or more residency/fellowship programs and may also be responsible for medical student elective clerkships in the Department.
Maintain contact with national accreditation association (AAALAC), oversee and contribute to the development and timely submission of the Institutional Animal Care and Use Program Description, and facilitate accreditation visits.
The Process Development Associate I will be responsible for upstream cell culture process development and downstream biologic purification activities such as the design and execution of laboratory experiments.
Assess eligibility of research subjects in accordance with the approved protocol and all applicable regulations including HIPAA. Assist PI in development of protocol-specific tools to aid in study documentation.
Coordinates the request for prior authorization (RPA) process including the data entry and the generation of reports that stem from this process, as well as ensure compliance with the federal twenty-four hour time limit.