In this role, the selected candidate will be working closely with a team of biologists, geneticists and bioinformaticians to apply functional genomic tools to address key questions about genetic targets and disease pathways.
In this role, you will be responsible for molecular characterization of proteins and lipids by mass spectrometry, including the development and implementation of analytical methodologies to support early research programs in a variety of disease areas.
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$45K to $75K -Princeton, NJ
This position is for an individual who has experience to coordinate and secure IRB approval (local and central). Responsible to provide step by step guidance and partnership with sites to secure IRB approval.
In this role, the selected candidate will
test standard procedures to provide recommendations for improvements. Contributes to information database development and suggests improvements to information systems
The employee will work in a project-focused environment as a member of an active, multidisciplinary group responsible for manufacturing process development of new products and optimization of established manufacturing procedures.
In this role, the selected candidate will be responsible for Contributes to initiatives for process improvement and consistency regarding aggregate reporting, signal management and responding to ad hoc safety questions.
The Sr. Scientist will be accountable to provide technical expertise to successfully execute the strategies leading to growth or maintenance of business in Coatings, Adhesives, Specialties (CAS) group.
In this role, you will investigate various receptors/ligands, and downstream signaling molecules, such as kinases, transcription factors, enzymes, and epigenetic regulators, and assess their potential therapeutic utility.
In this role, the successful candidate will be responsible for overseeing design and execution of in vivo studies, standardization of in vivo models, and development and characterization of new models to support project advancement as necessary.
In this role, you will develop efficient, appropriate formulation procedures for assigned compounds & aware of project needs to scope, write proposals, develop experimental details, GMP activities and timelines.
he successful candidate will identify, develop and validate relevant in-vivo models across a range of diseases to evaluate therapeutic candidates for proof-of-concept, mechanism of action, pharmacokinetics & pharmacodynamics, benchmarking and efficacy assessment.