Job Type: Full-Time / Part-Time / Contract Location: Multiple (Denver, CO & Illinois) Schedule: Flexible Part-Time (0-8 hours/week) or Full-Time options Compensation: Based on specialty, experience, and contract type Job Summary: We are seeking board-certified physicians across multiple specialties to serve as Clinical Research Physicians (Principal Investigator or Sub-Investigator). This is an excellent opportunity for physicians passionate about advancing medicine through research while maintaining a flexible schedule. Specialties of Interest Dermatology Cardiology Endocrinology Gastroenterology Hematology Infectious Disease Nephrology Neurology Oncology Obesity Medicine Pain Management PM&R Psychiatry Pulmonology Rheumatology Surgery (General & Subspecialties: Orthopedic, Cardiothoracic, etc.) Urology GI Key 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, and institutional guidelines. Stay updated on clinical research practices and therapeutic advancements. Requirements MD or DO degree with an active, unrestricted U.S. medical license (Colorado and/or Illinois preferred). Board certification in Dermatology or one of the listed specialties. DEA license and BLS/ACLS certification preferred. Prior clinical research experience strongly preferred (training available for motivated candidates). Proficiency with EHR, EDC, CTMS, and medical documentation systems. Strong communication and interpersonal skills; ability to thrive in a multidisciplinary, fast-paced environment. Commitment to ethical research and patient-centered care. Compensation & Benefits Flexible scheduling: 0-8 hours/week part-time or full-time options. Opportunity to participate in cutting-edge clinical trials across multiple therapeutic areas. Professional growth in research leadership and investigator experience. #J-18808-Ljbffr
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