In this role, you will be responsible to performs research; analysis; development and evaluation of systems; procedures and models in assigned functional area. Analyzes and defines problems and researches possible solutions that afford maximum probability for profit or effectiveness in relation to cost or risk.
In this role, the selected candidate will be responsible for the cold call as appropriate within your market or geographic area to ensure a robust pipeline of opportunities; meet potential clients by growing, maintaining, and leveraging your network.
In this role, the selected candidate will support the goals of the Gen Med organization by initiating, monitoring, and closing out clinical study sites following GCP and ICH guidelines as well as Novartis SOPs and ensuring that study milestones are met.
In this role, you will be responsible for coordinating the research activities of assigned IRB-approved study protocols Reports and is responsible to the Principal Investigator (PI) and supports the CID department head in accordance with federal and local regulatory guidelines.
CRNC is responsible for coordinating the research activities of IRB-approved study protocols. Specific protocols that require the CRNCs support will be determined by the Department Head of Clinical Investigation Department (CID) in consultation with the Clinical Research Coordinator.
In this role, the selected candidate will be responsible for the regulatory and scientific conduct of assay design and development, development, method development and validation, bioanalytical projects, and/or other specialty technologies.
In this role, the selected candidate will analyze large data sets and develop automated analytics to assist decision makers with making sense of data affecting DoD operations; develop machine learning, data mining, statistical, and graph.
This position will be responsible for the clinical management of research within the company to include coordination of all human subjects research/IRB, participation in initial and ongoing site visits and audits, management of multiple protocols involving patient screening, enrollment, treatment and education as well as coordination of patient care to adhere to timelines of clinical trials.
In this role, you will perform a variety of complex sample preparation and analysis procedures to quantitatively measure pharmaceutical and biopharmaceutical compounds in a variety of formulations and/or biological matrices.
In this role, you will be applicable to the phase of development, from pre-clinical all the way to development of the commercial dosage form and launch. Develops placebos for the product and comparative agents.