Research Senior Associate, Oncology Drug Discovery Unit

Company: Takeda Pharmaceutical
Location: Boston
Posted on: November 19, 2024

Job Description:

By clicking the "Apply" button, I understand that my employment application process with Takeda will commence and that the information I provide in my application will be processed in line with Takeda's Privacy Notice and Terms of Use. I further attest that all information I submit in my employment application is true to the best of my knowledge.Job DescriptionAre you looking for a patient-focused, innovation-driven company that will inspire you and empower you to shine? Join us as a Research Senior Associate, Oncology Drug Discovery Unit in our Cambridge office.At Takeda, we are transforming the pharmaceutical industry through our R&D-driven market leadership and being a values-led company. To do this, we empower our people to realize their potential through life-changing work. Certified as a Global Top Employer, we offer stimulating careers, encourage innovation, and strive for excellence in everything we do. We foster an inclusive, collaborative workplace, in which our global teams are united by an unwavering commitment to deliver Better Health and a Brighter Future to people around the world.Here, you will be a vital contributor to our inspiring, bold mission.Objective / Purpose:

• Provides onsite in vivo technical support, implementation, and coordination for research project teams across the department. This is a full-time position that requires onsite work on both Saturday and Sunday, as well as three additional weekdays. The focus is on the ability to independently and successfully execute key tasks for multiple studies.
• Provides technical and conceptual input into the design and development of well-defined studies. Independently executes on these studies, performs data analysis and presents the results and recommendations to the project team.
• Contributes from the lab to advance novel and differentiated therapeutic modalities towards preclinical and clinical milestones, by working collaboratively with internal cross-functional teams and external partners.Accountabilities:
  • Proper handling and care of mice and other rodents, tumor implantation, general dosing (multiple routes - oral, IV, IP, SC), collection and analysis of blood and tissue samples; work schedule flexibility, including a commitment to work weekends, to ensure optimal dosing schedules on a project-specific need will be required
  • Understands and implements study protocols in accordance with regulatory requirements for compliance with IACUC guidelines
  • Primary support for all weekend in vivo work for project teams across the department, including addressing and resolving technical issues that arise, maintaining a high level of scientific rigor and professionalism at all times.
  • Handles weekday responsibilities including (but not limited to) contributions to ongoing in vivo work as needed, administrative tasks, preparation for weekend activities, and team meetings.
  • Collaborates with team members across multiple project teams to create a seamless transition between weekday and weekend operations; Able to clarify requests and provide suggestions and put data into context.
  • Organize time and plan specifics of project related work with oversight from manager or project representative
  • Contributes to the design and execution of in vivo experiments, independently conducts complex experiments, exercising judgment to evaluate various technical factors and achieve optimal solutions, analyze and interpret data, and present results to stakeholders; Knowledge of data analysis programs such as GraphPad PRISM, Microsoft Excel, FlowJo FACS analysis, Nanostring transcriptome analysis and Softmax Pro and/or other equivalent software ideal but not required.
  • Independently provides work group with technical guidance and problem resolution related to methods, procedures and processes
  • Troubleshoots non-routine methods, instrumentation, or software issues and recommends systems, processes, or changes within project scope to meet objectives.
  • Utilizes assigned literature to increase knowledge base and implement improvements.
  • Maintains quality electronic laboratory notebook records and technical reports to support regulatory submissions as needed. - - - -Education & Competencies (Technical and Behavioral):
    • MS in a scientific discipline (or equivalent) with 1+ years relevant experience, or BS with 3+ years relevant experience
    • Experience with data analysis software, such as FlowJo and GraphPad Prism.
    • Good communications skills, both oral and written.
    • Excellent analytical, organizational, interpersonal and time management skills.
    • Strong team player who thrives in a dynamic, 'biotech-like' environment.Takeda is proud in its commitment to creating a diverse workforce and providing equal employment opportunities to all employees and applicants for employment without regard to race, color, religion, sex, sexual orientation, gender identity, gender expression, parental status, national origin, age, disability, citizenship status, genetic information or characteristics, marital status, status as a Vietnam era veteran, special disabled veteran, or other protected veteran in accordance with applicable federal, state and local laws, and any other characteristic protected by lawThis position is currently classified as "hybrid" in accordance with Takeda's Hybrid and Remote Work policy. -#LI-JT1Takeda Compensation and Benefits SummaryWe understand compensation is an important factor as you consider the next step in your career. We are committed to equitable pay for all employees, and we strive to be more transparent with our pay practices. -For Location:Boston, MAU.S. Base Salary Range:The estimated salary range reflects an anticipated range for this position. The actual base salary offered may depend on a variety of factors, including the qualifications of the individual applicant for the position, years of relevant experience, specific and unique skills, level of education attained, certifications or other professional licenses held, and the location in which the applicant lives and/or from which they will be performing the job.---The actual base salary offered will be in accordance with state or local minimum wage requirements for the job location. -U.S. based employees may be eligible for short-term and/ or long-term incentives. U.S. based employees may be eligible to participate in medical, dental, vision insurance, a 401(k) plan and company match, short-term and long-term disability coverage, basic life insurance, a tuition reimbursement program, paid volunteer time off, company holidays, and well-being benefits, among others. U.S. based employees are also eligible to receive, per calendar year, up to 80 hours of sick time, and new hires are eligible to accrue up to 120 hours of paid vacation. -EEO StatementTakeda is proud in its commitment to creating a diverse workforce and providing equal employment opportunities to all employees and applicants for employment without regard to race, color, religion, sex, sexual orientation, gender identity, gender expression, parental status, national origin, age, disability, citizenship status, genetic information or characteristics, marital status, status as a Vietnam era veteran, special disabled veteran, or other protected veteran in accordance with applicable federal, state and local laws, and any other characteristic protected by law.LocationsBoston, MAWorker TypeEmployeeWorker Sub-TypeRegularTime TypeFull timeJob ExemptYes

Keywords: Takeda Pharmaceutical, Plymouth , Research Senior Associate, Oncology Drug Discovery Unit, Other , Boston, Massachusetts