Study Director

Summary The position has responsibilities centered around the execution, planning, and management of assigned studies. The role will participate in vivo pharmacology research conducting biochemical screening models, proof-of-concept models for target validation, as well as disease efficacy models to evaluate development and discovery lead compounds. The ability to communicate succinctly with clients, coordinators, and technicians is key as well as a cross-functional, flexible, and collaborative spirit. Responsibilities Manages client correspondence and relationship Works with study sponsors to create study protocols Informs Live Phase Study Coordinator of decisions to initiate studies and thereby proceed with ordering animals and necessary study supplies Ensures all research technicians are properly trained to perform task and is ultimately responsible for all work performed on his/her study. Performs disease-inducing procedures Provides potential study sponsors with quotes for proposed studies Ensures all tasks are performed on daily schedule Performs surgical procedures Performs research technicians’ tasks, as needed Prepares high quality and accurate data package for clients Keeps track of project timelines for forecasting purposes Oversees coordinating of all studies and allocates resources Identifies and is accountable for driving ways to improve the efficiency and quality of processes and the resulting deliverables, influencing key stakeholders as applicable Writes IACUC protocols Other duties may be assigned Qualifications An individual with an in-depth understanding of  in vivo  models of multi-system rodent physiology and  in vitro  analyses of pathobiology and disease biomarkers. Demonstrates strong organizational, communication (both oral and written), time management, and interpersonal skills in a cross-functional team. Must actively participate and work well in a collaborative, team-oriented environment. Experience with rodent cardiac survival surgeries and/or cardiac ultrasound is required. Should be adept at data management and reduction. Able to demonstrate strong skills in authoring and managing the production of scientific documents (e.g., pre-clinical study protocols, data package, technical reports, publications in peer-reviewed journals). Proficient with Microsoft Excel, Word, and PowerPoint; familiarity with GraphPad Prism desired. Shows flexibility and ability to apply his/her knowledge to new areas of study. Commitment to safety and the humane treatment of laboratory animals is required. Minimum Education / Experience Requirements: A basic understanding of integrated physiology, pathophysiology, and pharmacology is required. Previous pre-clinical in vivo laboratory experience including handling of research rodents is required. Demonstrated ability to perform rodent cardiac survival surgeries and/or cardiac ultrasound is required. Industry research experience…