Educates patients about drug use and disease state management, including self-monitoring, dietary considerations, warning signs, etc. Updates case report forms and source documents in a timely and accurate manner.
Develop the health services research program. Facilitates and independently conducts academic/clinical research, supports research utilization in nursing/clinical practice and develops an ongoing strategic plan for academic/clinical research.
To address these questions, we utilize an array of molecular/cellular biology and immunology approaches in combination with genetic mouse models, Zebra fish, human cardiac tissue specimens, and human induced pluripotent stem cell (iPSC)-derived macrophages.
In this role, the selected candidate will require track record in piezoelectric dispensing of proteins from borosilicate glass capillaries onto substrate for protein biochip fabrication, I.e. printing immobilized protein macroarrays on substrates.
Standard molecular biology techniques such as molecular cloning, PCR, qRT-PCR, handling of retroviruses and lentiviruses, preparation and extraction of genomic DNA, RNA, Western blots, immunoprecipitation, in vitro binding assays, and ELISA.
The Clinical Research Associate (CRA), Oncology will monitor the progress of clinical studies at investigative sites or remotely, and ensure clinical trials are conducted, recorded, and reported in accordance with the protocol, standard operating procedures (SOPs), ICH-GCP, and all applicable regulatory requirements.
Successful candidates will be strategic, self-motivated, creative, efficient, and will have superior organizational and detail skills. This individual must have an interest in recruiting and research and have the ability to manage multiple projects and deadlines.
Position assist investigators as coordinator of a basic to moderately complex clinical research study; may be responsible for multiple research studies simultaneously, acting as a liaison with the school, sponsoring agency, community and the study participants; responsible for managing and recording all phases of study protocol as required by sponsoring agency to ensure compliance.
The role is in support of products and process development for biotherapeutics and vaccines, including antibodies, antibody-drug conjugates, and therapeutic proteins, in late-stage clinical development. The candidate will work across analytical functions, projects, and global sites.
The Credit Research Analyst is a member of the Credit Research Team within the Portfolio Management Group.Collectively, the Portfolio Management Group is responsible for all credit investment and portfolio management activities. Bottom-up, fundamentally driven analysis and relative value opinions are at the core of the Credit Research Teams contribution.
The chosen candidate will be responsible for process development, scale-up, technology transfer, establishing and optimizing commercial manufacturing processes for compounding and filling of solids, soft-chews, non-sterile liquids and sterile inject (aseptic manufacturing) platforms, as well as collaborating and partnering with Manufacturing, Engineering, and Quality organizations.