Preclinical Research Study Director

Position Title: Preclinical Research Study Director

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.

Salary Range
: $65,000 - $110,000 / annualy, DOE

• 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, and coordinate third-party reporting deliverables
• Collaborate with internal teams to maintain research quality, operational efficiency, and client satisfaction

• 5+ years of experience in a GLP-compliant laboratory or comparable regulated research environment
• Demonstrated experience developing scientific study protocols and writing detailed technical reports
• Strong understanding of laboratory research procedures, regulatory compliance, and scientific documentation
• Ability to manage multiple complex studies simultaneously while maintaining accuracy and meeting deadlines
• Excellent written and verbal communication skills, including experience communicating directly with clients
• Strong analytical, organizational, and problem-solving abilities
• Proficiency in Microsoft Office applications
• Ability to collaborate effectively with multidisciplinary research teams and incorporate constructive feedback
• Bachelor's or master's degree in a scientific discipline preferred; equivalent relevant experience will be considered
• Experience developing protocols and reports for animal studies strongly preferred
• Experience with preclinical research involving rabbits, pigs, sheep, goats, or rodents preferred

• 100% employer-paid medical, dental, and vision insurance premiums for employees and dependents
• Medical plan options, including high-deductible and low-deductible plans
• Employer HSA contributions of $100 per month for individual coverage or $200 per month for family coverage
• 401(k) retirement plan with a 4% company match
• 10 days of paid time off and 10 days of paid sick leave to start, with additional time off based on tenure
• 12 paid holidays annually
• $40 monthly wellness reimbursement
• Flexible start and end times within a Monday-Friday schedule
• Professional development, internal training, and opportunities for career advancement
• Fully stocked break room with complimentary snacks and beverages
• Company-sponsored celebrations and team events