Caribou Biosciences

Medical Director

• Establish, direct, and manage clinical efforts for multiple preclinical programs
• Lead the direction, planning, execution, and interpretation of clinical trials
• Establish scientific methods for clinical protocol design and implementation while ensuring trial subject safety
• Lead Phase I–IV clinical trials for company products
• Build and manage the clinical research scientist team supporting trials
• Oversee CROs and other vendors
• Develop relationships with clinical investigators and lead investigator meetings and advisory boards
• Monitor safety and report adverse events
• Coordinate information for FDA and other health authority reports and represent the company at forums
• Monitor protocol adherence and determine study completion
• Review clinical data and lead or author study reports, protocols, publications, IBs, and regulatory filings, including briefing documents and IND/BLA submissions
• Evaluate products for in-licensing or out-licensing
• Participate in cross-functional, highly matrixed teams to advance preclinical programs to clinical evaluation
• Monitor competitive clinical development and regulatory issues and recommend strategy or plan changes
• Provide medical review, assessment, and interpretation of clinical data in clinical study reports
• Adhere to GCP and GVP aligned with ICH requirements
• Ensure compliance with internal SOPs, local regulations, laws, and the highest ethical standards

• Serve as a medical advocate for Caribou, using disease-state knowledge and understanding of investigational cellular therapies during scientific exchange with healthcare providers
• Identify, build, and maintain relationships with clinical investigators, key opinion leaders, and academic research personnel
• Engage and educate pivotal trial sites at academic and community centers to support start-up activities
• Prioritize solutions to challenging scenarios and develop mitigation strategies for healthcare-team needs
• Support medical affairs projects including trial protocol development, publication support, and training
• Escalate issues to senior leaders as needed
• Provide clear, detailed, and regular communication to the headquarters medical team
• Deliver complex medical and scientific information effectively to healthcare providers

Medical Director

Senior Medical Science Liaison – Field Medical Affairs Director