Preclinical Research Study Director
About the role
We are seeking a Preclinical Research Study Director to oversee the planning, execution, and reporting of preclinical research studies in a GLP-compliant laboratory environment. This role serves as the primary point of contact for clients, develops study protocols, coordinates cross-functional teams, monitors study progress, and prepares comprehensive final reports. The Study Director will manage multiple studies simultaneously, ensuring scientific accuracy, regulatory compliance, and timely delivery of results. The ideal candidate has a strong background in regulated laboratory research, exceptional scientific writing skills, and experience developing protocols and reports. They are highly organized, collaborative, and comfortable managing competing priorities while maintaining the highest standards of scientific integrity and animal welfare.
Responsibilities
- Direct multiple preclinical research studies from protocol development through final reporting
- Develop detailed study protocols, research frameworks, and comprehensive scientific reports
- Serve as the primary client contact, communicating study progress, findings, deviations, and changes
- Coordinate with laboratory technicians, project coordinators, quality assurance teams, and external vendors to ensure successful study execution
- Interpret and analyze study data to produce accurate, scientifically sound final reports
- Ensure all studies adhere to Good Laboratory Practice (GLP) standards, established protocols, and applicable regulatory requirements
- Provide study-specific training and communicate specialized safety requirements to research teams
- Oversee approximately 12 concurrent studies across various stages of development and completion
- Monitor project timelines, address operational challenges,