Initiates and completes routine in vivo studies in an independent and efficient manner, with minimal supervision. Demonstrates the ability to interpret outcome of experiments and to propose appropriate follow-up; troubleshoots effectively
Demonstrates technical ability to assist in the design and execution of non-routine experiments in the context of cardio-renal-metabolic in vivo models; conducts exploratory experiments with minimal supervision.
Complies with applicable regulations including IACUC governance, performing all work in a safe and compliant manner; maintains proper records in accordance with Standard Operating Procedures and policies.
Applies basic scientific principles for study design, data analysis, and interpretation; performs literature searches and extracts relevant information from published protocols.
Independently operates and is responsible for lab equipment; troubleshoots effectively.
Communicates own work effectively orally and in writing; contributes to writing protocols, procedures, and technical reports; provide input for scientific reports.
Reports and treats data with a high level of integrity and ethics.
Skills:
Apply knowledge of basic theory and scientific principles of cardio-renal-metabolic diseases for conducting in vivo research; direct experience in rodent models of metabolic-associated steatohepatitis and liver fibrosis is desirable.
Experience in routine routes of rodent dosing (i.v., i.p., p.o., s.c., and i.m.), health monitoring, and sample collection is required.
Compliance and communication experience with IACUC governance.
Proven problem-solving ability with aptitude for agile learning style.
Assist in the incorporation of new technologies to enhance cardio-renal-metabolic research. Ability to contribute to the design, execution, and interpretation of non-routine experiments with minimal supervision and assist to the implementation of experimental approaches that contribute to department goals.
Communicates own work effectively orally and in writing; contributes to writing protocols, procedures, and technical reports; provide input for scientific reports.
Proficiency with computers and data analysis software such as Microsoft Excel and GraphPad Prism.
Ability and willingness to work effectively in a highly collaborative environment.
Education:
Master's Degree or Bachelor's Degree with 3+ years experience in related scientific discipline; pharmaceutical, biotechnology or CRO experience is highly desirable; non-PhD applicant required.