Company Description Powered Research, LLC is a leading preclinical contract research organization (CRO) specializing in non-GLP ophthalmology and oncology models for life science R&D companies. Based at a single site in Durham, NC, the company’s team of approximately 70 scientists, veterinarians, and technical experts has led thousands of preclinical studies with high scientific rigor. Powered Research focuses on transforming early discoveries into validated product candidates through collaborative, world-class preclinical research. Guided by integrity, excellence, and a commitment to improving human health, the organization aims to be the premier global partner for comprehensive preclinical research. Sponsors can easily access Powered Research’s ophthalmology and oncology services through its Science Exchange storefront for streamlined collaboration and project management.
Role Description The Preclinical Study Project Manager is a full-time, on-site role based in Durham, NC. This position is responsible for planning, coordinating, and overseeing preclinical ophthalmology and oncology studies from initiation through completion, ensuring timelines, quality standards, and Sponsor expectations are met. Day-to-day activities include developing study plans and schedules, tracking milestones, managing resources, monitoring study progress, and proactively resolving operational issues. The role involves close collaboration with scientists, veterinarians, technicians, and external Sponsors to clarify requirements, align expectations, and maintain clear communication throughout the study lifecycle. The Preclinical Study Project Manager will also support logistics related to materials, equipment, and samples, coordinate inspections and internal reviews as needed, and contribute to process improvements that enhance study efficiency and data quality.
Qualifications
- Demonstrated project management skills, including experience planning, tracking, and delivering complex scientific or technical projects (e.g., Project Management, Expeditor, Expediting).
- Experience coordinating logistics in a non-clinical research or laboratory setting, including scheduling, materials handling, and vendor or Sponsor coordination (e.g., Logistics Management, Expediting).
- Familiarity with inspection, quality checks, or compliance processes in a scientific, preclinical, or laboratory environment (e.g., Inspection).
- Strong organizational, time-management, and prioritization abilities with attention to detail and accuracy in documentation.
- Excellent written and verbal communication skills, with the ability to interface effectively with cross-functional teams and external Sponsors.
- Bachelor’s degree in a life science, veterinary science, or related field; advanced degree or equivalent relevant experience in preclinical research is a plus.
- Previous experience in a CRO, pharmaceutical, biotechnology, or preclinical research environment, particularly in ophthalmology or oncology, is highly beneficial.
- Proficiency with project management and collaboration tools, and comfort working in a fast-paced, deadline-driven setting.