Part-Time Clinical Research Gastroenterologist — PI/Sub-I

ProTouch Staffing; Chicago (IL); On-site; USD 207,000 - 289,000; Part time

Benefits offered by this job

Flexible schedule

Part-time opportunity

Research exposure

Job summary

ProTouch Staffing seeks a Board-Certified Gastroenterologist for a Chicago, IL-based clinical research role. This part-time position (0-8 hours per week) focuses on ensuring protocol compliance, patient safety, and high-quality data collection across Phase I-IV trials.

You will serve as PI or Sub-I where needed, perform screenings and exams, collaborate with sponsors and site teams, and stay current with regulations, EHR/EDC systems, and evolving therapeutic advances.

Qualifications

• MD/DO with active Illinois medical license.
• Board Certification in Gastroenterology.
• DEA license and BLS/ACLS certification.
• Clinical trials experience preferred (training available for motivated candidates).

Responsibilities

• Serve as Principal Investigator (PI) or Sub-Investigator (Sub-I) for clinical trials.
• Conduct medical screenings, physical exams, and assessments of study participants.
• Provide clinical oversight and ensure adherence to study protocols, ICH-GCP, and regulatory standards.
• Collaborate with coordinators, nurses, and research staff to maintain compliance and accurate documentation.
• Record patient interactions, manage adverse events (AEs/SAEs), and maintain compliance with EHR/EDC systems.
• Build and maintain strong relationships with sponsors, CROs, monitors, and IRBs.
• Participate in site initiation visits (SIVs), monitoring visits, audits, and investigator meetings.
• Contribute to feasibility reviews, study design, and recruitment strategies.
• Stay current with clinical research regulations and therapeutic advances.

Skills

Board Certification: Gastroenterology

Active Illinois medical license

DEA license

BLS/ACLS certification

Clinical trials experience

Education

MD/DO degree

Job description

ProTouch Staffing seeks a Board-Certified Gastroenterologist for a Chicago, IL-based clinical research role. This part-time position (0-8 hours per week) focuses on ensuring protocol compliance, patient safety, and high-quality data collection across Phase I-IV trials.

You will serve as PI or Sub-I where needed, perform screenings and exams, collaborate with sponsors and site teams, and stay current with regulations, EHR/EDC systems, and evolving therapeutic advances.