Manager, Research – Cardiovascular Research Foundation – Orangeburg, NY

Job title: Manager, Research Company: Cardiovascular Research Foundation Job description: All CRF employees must provide proof they have been fully vaccinated against COVID-19 or have a valid exemption from being vaccinated. SUMMARY Under supervision of Senior Director of Research conducts nonclinical research activities on behalf of Foundation in the field of experimental cardiovascular medicine; responsible for overseeing and directing the daily research operations at SCI. ESSENTIAL DUTIES AND RESPONSIBILITIES • Under direction of the Senior Director of Research, participates in and conducts nonclinical research activities on behalf of Foundation in the field of experimental medicine. • Participates in the initiation, design, development, execution, implementation and report writing of scientific research projects. • At the discretion of and under the supervision of the Senior Director of Research, manages a study from inception to completion, including protocol development, sponsor interface, liaison to scheduling team, arrangement of necessary equipment in-house and from external vendors, and sponsor follow-up. • Serves as liaison to the SCI operations team in the areas of allocating proper resources (human and material) for the studies. • Investigates the feasibility of applying scientific principles and concepts to potential technologies, materials, processes and products. Plans and executes laboratory research to prove feasibility of concepts. • Interfaces with Sponsors, suppliers and vendors. • Maintains substantial knowledge of state-of-the-art principles and theories, reviews technical journals, actively participates in exchange of project findings by attending and/or contributing to conferences and the peer reviewed scientific literature/community with papers, abstracts and presentations. • Attends relevant external events to promote the interests of Foundation. • Maintains subject matter expertise of regulatory agency requirements for Good Laboratory Practices (GLP) and quality control. • Ensures proper respect for and humane care and handling of research animals in accordance with institutional, USDA and AAALAC accreditation standard operating procedures. • Operates experimental imaging, physiology and other data-collecting instrumentation, if applicable. • Compiles, analyzes and interprets imaging and physiology data. • Works closely with the Senior Director of Research and other in-house and external experts to develop and improve experimental models, techniques and technologies. • Performs data processing, computational analysis, and modeling under the guidance of Senior Director of Research. • Works on a computer to enter, manipulate, save, and back up data and information using a variety of data processing, graphic communication, and web-based computer programs. • Leads necropsies, grossing and histology processing, if applicable. • Oversees sample collection, labeling, storage and shipment. • Works closely with Senior Director of Research and other in-house and external experts to develop and improve pathology techniques and technologies, if applicable. • Serves as a subject matter expert on, and liaison to Notocord for operation, maintenance, compliance and training of employees. • Additional duties as assigned. DUTIES AND RESPONSIBILITIES IN GLP STUDIES • Serves as GLP Study Director. • Leads study protocol development, approval and amendment. • Operates experimental imaging, physiology and other data-collecting instrumentation, if applicable. • Compiles, analyzes and interprets imaging and physiology data. • Performs data processing, computational analysis, and modeling under the guidance of Senior Director of Research. • Works on a computer to enter, manipulate, save, and back up data and information using a variety of data processing, graphic communication, and web-based computer programs. • Leads or supports necropsies, grossing and histology processing, if applicable. • Oversees sample collection, labeling, storage and shipment. • Executes the technical conduct of the study, documentation, analysis, interpretation and reporting of results, as appropriate. • Assures all study data are accurately recorded, reported and verified. • Leads study report preparation and delivery. • Documents any circumstances that may affect the quality and integrity of the study when they occur and assesses the impacts on the study outcome. • Assures corrective actions are taken and documented. QUALIFICATIONS • BS at minimum. • Minimum 5 years of experience in preclinical translational research required, including serving as a non-GLP and GLP study director. • Pathology/necropsy experience and/or cardiovascular research experience required. • Proficient in Microsoft Excel, Word, Power Point and Outlook. • Strong focus on flexibility, ability to multi-task, attention to detail, excellent organizational skills, good follow-up and judgment. Must be able to prioritize. • Must possess excellent communication and writing skills, patience, professionalism and ability to effectively interact with staff and management alike. • Ability to analyze complex information and solve problems relating to cardiovascular research. BENEFITS • Choice of health plans include medical, Dental, and vision coverage • Company-paid short-term and long-term disability and life insurance • Health and dependent care flexible spending accounts • Pre-tax travel expenses through TransitChek program • 401(k) plan • Generous paid time off (PTO) • Ten paid holidays each year CONTACT INFORMATION To be considered for this opportunity, please submit your resume. Be sure and visit our web site to learn more about how we strive to enhance and save patient lives every day www.crf.org CRF is an equal opportunity employer. Expected salary: Location: Orangeburg, NY Job date: Sun, 14 Aug 2022 07:53:48 GMT Apply for the job now! Apply tot his job