What are the responsibilities and job description for the Preclinical Study Coordinator/Project Manager position at Powered Research, LLC?
Company Description
Powered Research is a leading preclinical CRO specializing in non-GLP models for ophthalmology and oncology research. Established in 2012, the company is based in Durham, NC and has a team of 70 experienced domain experts who have led thousands of preclinical studies. Powered Research is committed to advancing scientific innovation with integrity and excellence, collaborating with life science R&D companies to deliver transformative therapies. By providing tailored solutions and prioritizing operational agility, the team directly impacts research pipelines and accelerates the journey from discovery to real-world solutions.
Role Description
This is a full-time, on-site role based in Durham, NC, for a Preclinical Study Coordinator/Project Manager. Responsibilities include overseeing preclinical studies in ophthalmology and oncology, coordinating timelines, ensuring compliance with internal and client requirements, and maintaining high scientific and operational standards. The role also involves acting as a primary liaison between teams, facilitating communication, managing resources, and supporting the training of team members. Additionally, the individual will be expected to contribute to processes and ensure seamless collaboration with Sponsors.
Qualifications
- Strong Project Management skills, including experience managing timelines, resources, and deliverables
- Effective Communication skills, with the ability to interface confidently and clearly with internal teams and Sponsors
- Proficiency in Research and Laboratory Skills, including executing preclinical protocols and ensuring scientific accuracy
- PMP certification preferred
- Attention to detail, organizational skills, and the ability to prioritize tasks effectively
- Bachelor’s degree in a life sciences field or related discipline is preferred
- Previous experience in a preclinical or research setting is highly desirable
- Proficiency with digital project management tools and familiarity with preclinical compliance standards is a plus