Title: Endocrinologist (Clinical Research)
Location: Denver, CO
Shift: Part-time (0-8 hours per week)

Responsibilities
• Serve as Principal Investigator (PI) or Sub-Investigator (Sub-I) on clinical trials.
• Conduct medical screenings, physical examinations, and specialty-specific evaluations for study participants.
• Provide medical oversight and ensure patient safety throughout all trial phases.
• Monitor, document, and report adverse events (AEs/SAEs) in compliance with study protocols and regulatory standards.
• Collaborate with study coordinators, research staff, sponsors, CROs, and IRBs to ensure protocol compliance and data quality.
• Participate in site initiation visits, monitoring visits, audits, and investigator meetings.
• Contribute to protocol feasibility reviews, recruitment strategies, and study design discussions.
• Maintain compliance with GCP, FDA regulations, ...