Gastroenterology Physician

Protouch Staffing; Carrollton (TX); On-site; USD 138,000 - 344,000; Part time

Benefits offered by this job

Flexible schedule

Competitive hourly rate

Job summary

Protouch Staffing seeks a board-certified Gastroenterologist to join a clinical research site in Carrollton, TX. This part-time role (0-8 hours/week) offers flexibility and a chance to lead clinical trials as PI or Sub-I.

The physician will perform screenings, exams, and safety monitoring, ensuring protocol compliance and accurate documentation with staff support. TX license and DEA required; BLS/ACLS certific.

Qualifications

• MD/DO with active Texas medical license and gastroenterology board certification.
• Valid DEA license and current BLS/ACLS certification.
• Clinical research experience preferred.

Responsibilities

• Serve as PI or Sub-I across clinical trials in diverse therapeutic areas.
• Conduct medical screenings, specialty assessments, and physical examinations.
• Ensure participant safety and protocol adherence per ICH-GCP and FDA standards.
• Collaborate with coordinators, nurses, and research staff for documentation and trial execution.
• Monitor adverse events and maintain compliant 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 input during feasibility reviews, recruitment strategies, and study design discussions.
• Stay updated on regulations and investigational therapies.

Skills

Communication skills

Interpersonal skills

Collaboration

Education

MD/DO degree

Texas medical license

Tools

EDC

CTMS

EHR systems

Job description

Clinical Research Physician (Gastroenterologist) – 8 hrs. per week Location: Carrollton, TX Schedule: Flexible Part-Time (0-8 hours per week) Start Date: Within 0-6 months About the Role We are seeking board-certified Gastroenterology to join our clinical research site. This part-time position offers physicians the opportunity to contribute to groundbreaking medical research while maintaining a flexible schedule. You will serve as a Principal Investigator (PI) or Sub-Investigator (Sub-I), overseeing clinical trial activities and ensuring the highest standards of patient safety and protocol compliance across Phase I-IV studies. Key Responsibilities Serve as PI or Sub-I across 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 Gastroenterology. 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). Strong communication and interpersonal skills with a collaborative mindset. Commitment to ethical, patient-centered research. 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.