Gastroenterology Physician

ProTouch Staffing; Denver (CO); On-site; USD 150,000 - 230,000; Full time

Benefits offered by this job

Flexible scheduling

Research opportunities

Professional growth

Job summary

ProTouch Staffing is seeking board-certified physicians to serve as Clinical Research Physicians (PI or Sub-I) across multiple specialties. This role offers flexibility with Part-Time or Full-Time options in Denver, CO and Illinois, and focuses on advancing medicine through research while maintaining a flexible schedule.

Ideal candidates hold an active U.S. medical license (Colorado/Illinois preferred), with board certification in listed specialties and experience in clinical research.

Qualifications

• MD or DO degree with 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.

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.

Skills

Clinical judgment

Communication skills

Team collaboration

Regulatory knowledge

Education

MD/DO degree

Tools

EHR

EDC

CTMS

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.