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Posted Job TitleResearch Specialist C/D (Center for Cellular Immunotherapy)Job Profile TitleResearch Specialist CJob Description SummaryThe Human Genome Editing Research Specialist will play a key role in managing the Human Genome Editing Lab (HGEL) at the Center for Cellular Immunotherapy (CCI) at the University of Pennsylvania. This individual will directly report to and assist the Director in laboratory management, and lead multiple research projects related to cell and gene therapy, and contribute to the development and implementation of assays for improving clinical cell products.Job DescriptionThe principal responsibilities encompass clinical-scale processing of cells, involving the isolation, genetic modification, expansion, formulation, and cryopreservation of specific human hematopoietic cell fractions. Additionally, the role involves the isolation, expansion, and cryopreservation of tumor cell populations. The incumbent will play a pivotal role in developing and implementing cell-based assays aimed at enhancing clinical cell products.
This position additionally requires providing technical support for in vitro and in vivo experiments, encompassing molecular biology, cell culture, and flow cytometry, for the benefit of post-doctoral fellows and graduate students within the laboratory. Beyond these duties, the individual will contribute to the development and validation of standard operating procedures (SOPs) critical for modifying and upscaling cell products in preparation for clinical manufacturing. This encompasses the execution of assays, data analysis, presentation of findings, and overall laboratory management, including the oversight of materials and equipment. Additionally, the role involves training others in various techniques and procedures and engaging with vendors.
Proficiency in handling and processing primary clinical samples, expertise in genetic engineering through viral or non-viral delivery methods, multi-color flow cytometry, general laboratory operations, and familiarity with animal experimentation are prerequisites for this position. The successful candidate must possess extensive organizational skills, troubleshooting capabilities, effective communication skills, teamwork ethos, a commitment to accurate documentation, and a strong sense of personal responsibility.
This Human Genome Editing Research Specialist C/D position requires a dynamic individual with a strong background in genome editing, laboratory management, and collaborative research efforts in the field of cell and gene therapy. The ability to meet the specified qualifications is crucial for the success of this position in advancing the goals of the Center for Cellular Immunotherapy.
In addition, the Research Specialist D position requires an individual with advanced expertise, leadership capabilities, and a strategic vision to drive the laboratory's success. The increased level of responsibility involves leading complex projects, navigating regulatory landscapes, and contributing significantly to the advancement of the center's objectives.
Qualifications
Research Specialist C- Bachelor of Science and 3 to 5 years of experience or equivalent combination of education and experience is required.
Research Specialist D- Masters of Science in Biology and 3 to 5 years of experience or equivalent combination of education and experience is required. PhD preferred.
Additional Qualifications:
relevant experience in molecular biology, cell culture, flow cytometry, and human genome editing technique
Demonstrated experience in managing a laboratory and supporting multiple research projects
Proficiency in clinical-scale cell processing for isolation, genetic modification, expansion, formulation, and cryopreservation of human hematopoietic cell fractions
Expertise in isolation, expansion, and cryopreservation of tumor cell populations
Hands-on experience with in vitro and in vivo experiments, including molecular biology, cell culture, and flow cytometry
Proven track record of adherence to regulatory standards and guidelines, especially in the context of clinical cell product development
Experience in the development and implementation of assays supporting research activities
Ability to contribute to the development and validation of standard operating procedures (SOPs) for cell product modification and upscaling crucial for clinical manufacturing
Excellent written and verbal communication skills, with the ability to convey complex scientific information clearly to diverse audiences
Interpersonal skills to collaborate effectively with post-doctoral fellows, graduate students, and other team members
Strong organizational skills for the efficient management of laboratory space, equipment, software, protocols, and documentation
Experience in handling and processing primary clinical samples, genetic engineering using viral or non-viral delivery methods, and multi-color flow cytometry
Troubleshooting capabilities to address challenges related to laboratory operations, experimental procedures, and data analysis
Ability to work collaboratively in a team, including training others in techniques and procedures
Cross-functional collaboration with other labs for the translation of new processes and genetically-engineered cellular products to the clinic
Personal responsibility for accurate documentation, performance of assays, data analysis, and presentation of findings
This position is contingent upon grant funding.
Job Location - City, StatePhiladelphia, PennsylvaniaDepartment / SchoolPerelman School of MedicinePay Range$43,919.00 - $81,000.00 Annual RateSalary offers are made based on the candidate's qualifications, experience, skills, and education as they directly relate to the requirements of the position, as well as internal and market factors and grade profile. Affirmative Action Statement
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