Senior Associate Scientist

Job Overview Biomarkers (and Investigative Pathology) personnel are responsible for the development, performance, and support of biomarkers and flow cytometry-based assays. They assist in sample analysis for both internal studies and external client-based studies in a GLP compliant environment, including but not limited to cytokine, hormone, renal, cardiovascular, osteo, complement, metabolic, and inflammatory markers. Essential Functions Effectively manage a portfolio of sample analysis projects while ensuring timelines are met in a single operational area with oversight. Execute review and approval of data with oversight for final scientific/technical decisions within a single operational area. Develop understanding of compliance expectations to respond to quality assurance audit observations in appropriate software with oversight. Assist with oversight the completion of laboratory investigations, assay troubleshooting and quality observations. Assist in problem solving for technical and/or regulatory issues with oversight. Responsible for writing and preparing study plans/protocols/amendments with minimal oversight. Participate in sponsor visits/tours with minimal oversight. Develop expertise in developing and validating quantitative/qualitative methods/procedures with limited complexity/scope in one operational area with minimal oversight. Perform data analysis using appropriate software with minimal oversight. Develop critical thinking, troubleshooting and time management skills aligned with needs of operational areas. Demonstrate effective communication skills through informal discussions with peers, supervisor, and team. Function as a liaison, maintaining timely and frequent communication between CRL and sponsor/client/SD with minimal oversight. Ensure scientific integrity of studies with minimal oversight. Function as a Principal Investigator, Individual Scientist and/or Study Director as assigned with minimal oversight. Actively communicate and collaborate across operational areas to adhere to timelines and produce quality data. Efficiently perform and document all procedures, materials and results in compliance with applicable regulatory standards (protocols, methods, SOPs, etc.). Write, review and approve deviations with oversight. Develop knowledge of regulatory and GXP requirements, industry standards and company SOPs within one operational area. Effectively manage a small portfolio of research projects including method development and validation while ensuring timelines are met in a single operational area with oversight. Perform all other related duties as assigned. Job Requirements Bachelor’s degree (BA/BS) with 5-7 years of relevant working experience; Master’s degree (MS) with 1-2 years of relevant work experience; Doctorate degree (PhD) with no experience. CRO experience preferred. Experience with Luminex preferred. Ability to communicate verbally and in writing at all levels inside and outside the organization. Basic familiarity with Microsoft Office Suite. Computer skills commensurate with Essential Functions, including the ability to learn a validated system. Ability to work extended hours beyond normal schedule, including evenings, weekends, and short‑notice shifts. Ability to work under specific time constraints. Must be authorized to work in the United States without a sponsor visa, now or in the future. Physical Demands Perform general office and/or laboratory procedures, which require talking, hearing, standing, or sitting for long periods; typing/entering data into a computer; using instruments; reaching with hands and arms; wearing safety equipment (PPE) according to OSHA regulations. Specific vision abilities required: close vision, color vision, depth perception, and the ability to adjust focus. General office working conditions: noise level usually quiet. Occasional requirement to wear protective clothing (goggles, face shield, surgical mask, cap, scrubs, boots); work near toxic or caustic chemicals; work with biohazards or live animals with risk of exposure to allergens and/or zoonotic diseases. Occasional exposure to fumes or airborne particles, unpleasant odors, and/or wet, humid and/or extreme temperature conditions. The pay rate for this position is $80,000 per year. We’re committed to providing benefits that elevate your quality of life. Based on your position these may include: bonus/incentives based on performance, 401K, paid time off, stock purchase program, health and wellness coverage, employee and family well‑being support programs, and work‑life balance flexibility. Charles River is an equal‑opportunity employer and is committed to providing equal employment opportunities for all qualified applicants and employees without regard to race, color, sex, religion, national origin, ancestry, age, mental or physical disability, family status, pregnancy, military or veteran status, or any other characteristic protected by federal, state, or local laws. #J-18808-Ljbffr Charles River