Pre-clinical Lab Coordinator

Job Description The Pre‑clinical Lab Coordinator is a hands‑on operations lead responsible for coordinating and executing pre‑clinical lab activities. This role partners closely with cross‑functional stakeholders including Clinical Engineering, Product Development, Engineering and Research teams to ensure labs are properly scheduled, staffed, equipped, and successfully delivered. The Pre‑clinical Lab Coordinator serves as the bridge between planning and execution, owning lab operations while stepping in as a hands‑on operator for complex system setups, troubleshooting, and critical lab activities. Essential Job Responsibilities Lab scheduling system management Own and manage lab scheduling systems, request intake workflows, and tracking dashboards Maintain and enable cross‑functional visibility into lab demand, capacity, and upcoming studies Drive lab and specimen forecast planning activities working with cross‑functional stakeholders Identify and resolve scheduling conflicts, resource gaps, resource availability (prototype/system/sub‑system/animal/tissue) and operational risks working with cross‑functional stakeholders Align with cross‑functional stakeholders to ensure pre‑clinical labs are fully prepared ahead of execution (staffing, equipment, materials) Lab operations ownership & technician coordination Partner with Clinical Engineering team to ensure smooth day‑to‑day lab readiness and study execution Provide day‑to‑day task direction, prioritization, and coordination for lab technician(s) Ensure alignment of technician activities with lab priorities and execution timelines Ensure technician‑dependent tasks (setup, reprocessing, equipment prep) are completed Identify process gaps and create standard work instructions as needed for lab technician(s) to streamline and standardize Provide real‑time coordination and decision‑making support to lab technician(s) during execution Monitor quality and completeness of technician work Hands‑on lab support & technical leadership Provide hands‑on support for routine lab setup, equipment preparation, and troubleshooting; develop SOPs/playbooks for repeatability Support non‑routine or complex lab setups in collaboration with clinical engineering partners and help develop standardized workflows Step in to support clinical engineering team for lab execution during critical or resource‑constrained product development lab activities Resource planning & management Proactively review upcoming lab schedules to ensure alignment of people, equipment, and materials for lab execution readiness Maintain visibility into technician availability, equipment readiness, and supply status Identify and resolve resource gaps to ensure execution readiness Align lab demand with available capacity and elevate constraints as needed Equipment & lab readiness Ensure all lab equipment is available, functional, and ready for use Troubleshoot and resolve equipment issues, escalating when needed Coordinate maintenance and repairs with internal and external technicians and vendors as needed Ensure readiness of robotic systems, A/V setups and connectivity ahead of pre‑clinical lab execution Study coordination Coordinate lab readiness for onsite and offsite pre‑clinical studies in partnership with clinical engineering and supporting teams Align stakeholders on timelines, dependencies, and requirements Ensure materials, equipment, and setup requirements are met Track readiness across all components required for successful execution Training coordination Support planning and execution of training programs defined by Supervisor Coordinate training lab logistics, schedules, and participant tracking Manage training documentation and completion records Process improvement & operational efficiency Identify inefficiencies in lab workflows and execution processes Develop and maintain standardized workflows and playbooks to improve repeatability and reduce execution variability Propose and implement improvements to scheduling, coordination, and execution Create and manage dashboards to provide visibility into lab efficiency tracking Support adoption of tools and systems to improve lab operations Improve lab utilization, readiness, and execution consistency Cross‑functional collaboration and communication Act as central coordination point across engineering, research, and operations teams Communicate lab status, risks, and updates clearly and proactively Build strong relationships with engineers, technicians, and collaborators Qualifications Required Bachelor’s degree in Life Sciences, Biomedical Engineering, or related field 2–5 years of experience in lab operations, pre‑clinical research, or technical lab roles Strong hands‑on experience with lab equipment, set‑up, and troubleshooting Experience coordinating lab workflows or supporting multiple studies Ability to balance execution and coordination responsibilities Proficient in working with computer systems and office applications including Word, Excel, Smartsheet, etc. Preferred Experience in medical device or pre‑clinical lab environments Exposure to robotic or surgical systems Familiarity with regulated environments (e.g., IACUC, GLP‑adjacent) Key Skills Strong hands‑on technical capability Operational ownership and execution mindset Ability to balance coordination and execution Problem‑solving in dynamic lab environments Clear communication and stakeholder management Attention to detail and quality Travel up to 25% (domestic). Compensation Base Salary Range Region 1: $106,000 - $143,400 Base Salary Range Region 2: $90,100 - $121,900 Shift: Day Workplace Type: Onsite - This job is fully onsite. EEO Statement We are an AA/EEO/Veterans/Disabled employer. Intuitive is an Equal Opportunity Employer. We provide equal employment opportunities to all qualified applicants and employees, and prohibit discrimination and harassment of any type, without regard to race, sex, pregnancy, sexual orientation, gender identity, national origin, color, age, religion, protected veteran or disability status, genetic information or any other status protected under federal, state, or local applicable laws. Mandatory Notices U.S. Export Controls Disclaimer: In accordance with the U.S. Export Administration Regulations (15 CFR 743.13(b)), some roles at Intuitive Surgical may be subject to U.S. export controls for prospective employees who are nationals from countries currently on embargo or sanctions status. For any Intuitive role subject to export controls, final offers are contingent upon obtaining an approved export license and/or an executed TCP prior to the prospective employee’s start date, which may or may not be flexible, and within a timeframe that does not unreasonably impede the hiring need. If applicable, candidates will be notified and instructed on any requirements for these purposes. We will consider for employment qualified applicants with arrest and conviction records in accordance with fair chance laws. Preference will be given to qualified candidates who do not reside, or plan to reside, in Alabama, Arkansas, Delaware, Florida, Indiana, Iowa, Louisiana, Maryland, Mississippi, Missouri, Oklahoma, Pennsylvania, South Carolina, or Tennessee. This position may be filled at a different job level than listed here depending on business need and/or on the selected candidate’s experience, knowledge and skills. #J-18808-Ljbffr Intuitive