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.
