Job Description

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.

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