Gastroenterology Physician

ProTouch Staffing; San Antonio (TX); On-site; USD 138,000 - 344,000; Part time

Benefits offered by this job

Flexible part-time schedule

Opportunity to gain clinical research

Job summary

ProTouch Staffing in San Antonio, TX seeks a part-time Clinical Research Gastroenterologist to lead or co-lead trials (Phase I–IV) with flexible hours.

The physician will perform screenings, exams, and safety oversight, collaborating with research teams to ensure protocol compliance and accurate documentation.

Active Texas medical licensure, board-certified in gastroenterology, and clinical research experience are preferred; DEA and BLS/ACLS are required.

Qualifications

• MD or DO with active Texas medical license.
• Board-certified in Gastroenterology.
• DEA license and BLS/ACLS certification.
• Prior clinical research experience preferred (training available).
• Proficiency with EHR systems and clinical trial platforms (EDC, CTMS).

Responsibilities

• Serve as PI or Sub-I across Phase I-IV trials.
• Conduct medical screenings, exams, and specialty assessments.
• Ensure safety and protocol adherence per ICH-GCP and FDA.
• Collaborate with coordinators, nurses, and staff for documentation.
• Document patient interactions and monitor AEs/SAEs.
• Engage with sponsors, CROs, monitors, and IRBs.
• Participate in site initiation and monitoring visits.
• Contribute to feasibility reviews and study design discussions.

Skills

DEA license

BLS/ACLS

EHR experience

Education

MD/DO

Texas medical license

Board-certified in Gastroenterology

Tools

EDC

CTMS

Job description

Clinical Research Gastroenterologist – San Antonio, TX

Job Type: Part-time (0-8 hours per week, flexible schedule) Start Date: Within 0-6 months.

Responsibilities

• Serve as Principal Investigator (PI) or Sub-Investigator (Sub-I) across Phase I-IV clinical trials in diverse therapeutic areas.
• Conduct medical screenings, specialty assessments, and physical examinations.
• Ensure participant safety and protocol adherence in compliance with ICH-GCP, FDA, and regulatory standards.
• Collaborate with coordinators, nurses, and research staff for accurate documentation and trial execution.
• Document patient interactions, monitor adverse events (AEs/SAEs), and maintain compliance with EHR/EDC systems.
• Engage with sponsors, CROs, monitors, and IRBs to support trial success.
• Participate in site initiation visits, monitoring visits, and audits.
• Provide medical expertise during feasibility reviews, recruitment strategies, and study design discussions.
• Stay updated on clinical research regulations and advances in investigational therapies.

Qualifications

• M.D. or D.O. with an active, unrestricted Texas medical license.
• Board-certified in Gastro enterology.
• Valid DEA license and current BLS/ACLS certification.
• Prior clinical research experience preferred (training available).
• Proficiency with EHR systems and clinical trial platforms (EDC, CTMS).

Compensation & Benefits

• Competitive hourly rate: $100 – $250 based on specialty and experience.
• Highly flexible, part-time schedule (ideal for supplemental income or work-life balance).
• Gain or expand experience in clinical research.
• Contribute to the advancement of medical innovation and patient care.