• Oversee custom Antibody projects from intake to final delivery • Gather antibody design requirements • Prepare quotes and maintain real-time status updates • Serve as the primary contact for project timelines, data quality, and technical updates • Maintain precise records of quotes and orders in progress • Identify workflow inefficiencies and suggest ways to scale operations

- Oversee commercial electrical construction projects from preconstruction through final turnover and closeout - Manage project schedules, manpower planning, procurement activities, and field coordination across active job sites - Interface directly with clients, general contractors, inspectors, vendors, and internal operations teams throughout project execution - Review construction drawings, specifications, RFIs, submittals, and change orders to ensure project accuracy and execution - Track project budgets, forecasting, labor productivity, and cost exposure throughout the project lifecycle - Lead coordination efforts between field teams, BIM/VDC support, prefabrication, and estimating departments - Identify and resolve scheduling conflicts, field issues, material delays, and project risks before they impact delivery - Support subcontractor management, progress billing, and documentation requirements for commercial electrical projects - Maintain clear communication with leadership regarding project status, staffing needs, and operational challenges - Drive project execution across healthcare, institutional, industrial, and large commercial construction environments

Role Description WSP is seeking a Senior Environmental Planner to join our expanding Pacific Northwest Environmental Impact Assessment and Permitting service group. The position is either remote or hybrid working out of our Seattle, Redmond (WA), Bend, Portland or Boise offices. The position will be filled by a detail-oriented candidate, with strong writing skills and ability to manage multi-discipline work flows. The Senior Environmental Planner will lead environmental assessment, permitting and compliance services in support clients in the power, oil and gas, manufacturing, and data center sectors. This role will work closely with project managers to ensure environmental deliverables are prepared according to the quality, budget and schedule requirements. Your Impact - Leading and reviewing NEPA, SEPA, and/or CEQA environmental documents - Developing environmental compliance strategies and preparing documentation related to compliance with: - NEPA and SEPA - Energy Facility Siting in OR and WA (EFSC or EFSEC) - USFS Special Use Permits and forest management plans - BLM right-of-way agreements and resource management plans - Clean Water Act, Section 404/Section 401 - Land Use Planning Requirements in OR, WA, ID - Leading energy infrastructure routing and siting studies - Managing tasks or projects, including overseeing small project teams - Developing and managing scopes, schedules, budgets - Interfacing with clients, agencies, other consultants, and the public Qualifications - BS degree in Environmental Planning, Environmental Science, Environmental Engineering, Urban Planning, Landscape Architectural, or related degree - Minimum of five (5) years of post-education work experience - Experienced in developing environmental documentation related to NEPA, SEPA, CEQA, EFSC, and/or EFSEC compliance - Experienced in completing environmental permit applications and supporting analyses - Excellent written and verbal communication - Valid U.S. driver’s license and a satisfactory driving record for business travel Preferred Qualifications - AICP certified, or ability to obtain certification is a plus Benefits - Comprehensive suite of benefits focused on providing health and financial stability throughout the employee’s career - Coverage related to medical, dental, vision, disability, and life - Retirement savings - Paid sick leave - Paid vacation (or other personal time) - Paid parental leave - Paid time off for purposes of bereavement, voting, and/or attendance at naturalization proceedings Compensation Expected Salary (all locations): $74,200 - $133,500. WSP USA is providing the compensation range that the company in good faith believes it might pay and offer for this position, based on the successful applicant’s education, experience, knowledge, skills, abilities in addition to internal equity and specific geographic location. WSP USA reserves the right to ultimately pay more or less than the posted range and offer additional benefits and other compensation, depending on circumstances not related to an applicant’s sex or other status protected by local, state, and/or federal law.

• Lead internal research projects from initiation through completion, including scope definition, planning, execution, and documentation. • Track external collaborative research projects to develop and maintain study workflows, assess progress, proactively manage risks, and support timely data availability for analysis, publication and presentation at key congresses. • Ensure alignment on project goals, rationale, and roles & responsibilities with stakeholders and leadership. • Develop and maintain project charters, timelines and work plans, driving accountability across the team. • Facilitate clear communication across project teams, internal partners, functional leaders, and external collaborators. • Identify and manage risks and issues, proactively communicating and adjusting plans as needed. • Partner with other Program and Project Managers across Adaptive to support infrastructure for project management, prioritization, communication, and institutional knowledge sharing. • Participate in cross-functional initiatives as a contributing team member. • Perform / support analysis to inform business case and resource allocation • Define metrics for project success and determine how to measure • Provide regular reporting on project status to manager and project team, highlighting key risks, issues, and milestones. • Contribute to the development and execution of research studies that support MRD product and commercial strategy • Clinical study execution support: Track protocol development, contracting, study start-up, and coordinate cross-functional operational workflows (Regulatory/IRB, Clinical Trials, lab teams). • IRB protocol coordination: Facilitate IRB protocol submissions and related materials; track IRB protocol progress, approvals, and renewal dates; and coordinate record updates and amendments as required to ensure protocols do not lapse and study activities remain appropriately covered. • Visibility + stakeholder communication: Provide clear status reporting, surface critical-path risks, and align on mitigation/alternative plans with Medical Affairs leadership and key stakeholders. • Scientific output enablement: Track data generation and publication/congress timelines, maintain data-readiness visibility, and build/maintain tracking tools and outreach tracking for study opportunities/sites. • All other duties as assigned