Associate Scientist, Research Position Available In Hillsborough, Florida

Tallo's Job Summary: The Associate Scientist, Research role in Tampa, FL involves optimizing anti-tumor activity of tumor-infiltrating lymphocytes (TIL) through gene editing and viral vector production. Candidates need a Master's degree with 3+ years of experience or a Bachelor's degree with 5+ years of experience in relevant fields. Responsibilities include experimental design, vector production, gene editing, data analysis, and contributing to scientific publications. The role requires strong organizational, communication, and problem-solving skills.

Company:
Iovance Biotherapeutics
Salary:
JobFull-timeOnsite

Job Description

Associate Scientist, Research 2.0 2.0 out of 5 stars Tampa, FL 33612 Overview Associate Scientist will work on developing methods to optimize the anti-tumor activity of tumor-infiltrating lymphocytes (TIL) for therapeutic applications. Such methods include the use of gene editing, gene augmentation, and other ex vivo manipulations of TILs during the expansion process aiming at improving the function, trafficking, and persistence of TILs. The position requires prior experience working in a research laboratory. The ideal candidate will have experience with cellular assays, ddPCR, qPCR, other molecular biology techniques, knowledge of gene therapy and gene editing, and skills in viral vector production and analysis. This position requires an individual to be very motivated and bring impactful work to the team to help move new TIL approaches into the clinic. Essential Functions and Responsibilities Work as part of a research and development group to support ongoing projects in the lab. Design and execute experimental plans and protocols consistently. Produce and characterize viral vectors. Perform and analyze vector transduction and transgene expression. Deliver gene editing components using various approaches and assess editing efficiencies. Develop assays to evaluate functions of genetically modified TILs. Analyze and interpret experimental results. Make detailed observations and record them in a timely and relevant fashion. Capability for troubleshooting technical issues and presenting ideas to the team. Investigate and develop new methods and technologies necessary for project advancement. Write corresponding SOPs. Contribute to scientific publications and regulatory document writing. Help identify patentable inventions. Must adhere to Iovance Biotherapeutics’ core values, policies, procedures, and business ethics. Comply with Safety SOPs, SDS sheets, and laboratory procedures per company policy and OSHA regulations. Perform all other related duties as assigned Required Education, Skills, and Knowledge Master’s Degree (MS) in Cellular Biology, Molecular Biology, Immunology, or related discipline with 3+ years of relevant work experience (industrial experience preferred). Bachelor’s degree (BA/BS) in Cellular Biology, Molecular Biology, Immunology, or related discipline with 5+ years of relevant working experience (industrial experience preferred). High motivation and flexibility to adapt to new situations and be part of a dynamic and growing team. Extensive experience in viral vector production, characterization, and analysis is required. Skills in molecular biology, ddPCR or qPCR, gene editing, flow cytometry, tissue culture using primary and established cell lines, and immunological assays are preferred. Knowledge of gene therapy, gene editing, and cell therapy is preferred. Ability to independently carry out all lab experiments, analyze and interpret experimental results, make detailed observations, and record them in a timely and relevant fashion. Ability to organize presentation and discussion results and develop new methods and technologies necessary for project advancement. Excellent record-keeping and organization skills are needed. Must be able to communicate (verbal and written) effectively. Excellent collaborative style. Preferred Education, Skills, and Knowledge Ph.D. in Cellular Biology, Molecular Biology, Immunology, or related discipline with 0-2 years of post-doc or industry experience The physical demands described here represent those that an employee must meet to perform the essential functions of this job successfully. Reasonable accommodations may be made upon request to enable individuals to perform essential functions. Please contact Human Resources to request an accommodation. Physical Demands and Activities Required Must be able to move to and from the office to the lab located on separate floors and move about the office and lab as needed. Must be able to remain in a stationary position standing or sitting for prolonged periods of time. Must be able to grasp with both hands, perform repetitious actions such as pinch with thumb and forefinger, turn with hand/ arm, and reach above shoulder height. Must be able to use several types of laboratory equipment and pipettes for extended periods. Must be able to work on a tablet or computer typing for 50% of a typical working day. Must be able to move and lift 20 pounds multiple times daily. Must be able to use near vision to view samples at close range. Wear proper personal protective equipment when in a laboratory setting, i.e., safety glasses, lab coats, and closed-toed shoes.

Mental :

Clear and conceptual thinking ability; excellent judgment, troubleshooting, problem-solving, analysis, and discretion; ability to handle work-related stress; ability to handle multiple priorities simultaneously; and ability to meet deadlines Work Environment This position will work in both an office and a laboratory setting. When in the lab, there may be a risk of exposure to hazardous or biological waste within the environment through receipt, transport, storage, preparation, dispensing, administration, cleaning, and/or disposal of contaminated areas and waste. The statements contained in this document are intended to describe the general nature and level of work being performed by a colleague assigned to this description. They are not intended to constitute a comprehensive list of functions, duties, or local variances. Management retains the discretion to add or to change the duties of the position at any time. Iovance is committed to cultivating and offering a diverse and inclusive work environment. As an equal-opportunity employer, our employees and applicants will be considered without regard to an individual’s race, color, religion, sex, pregnancy, national origin, age, physical and mental disability, marital status, sexual orientation, gender identity, gender expression, genetic information, military and veteran status, and any other characteristic protected by applicable law. If you need assistance or accommodation to apply to one of our opportunities, please contact hr@iovance.com. By voluntarily providing information and clicking “Submit Application”, you explicitly consent to the collection and use of your personal information for the purposes described above and in our Candidate Privacy Notice. #LI-onsite

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