Protouch Staffing
Job Title: Part-Time Clinical Research Gastroenterologist
Location: Scottsdale, AZ
Schedule: Part-Time (0 8 hours / week)
Start Date: Within 0 6 months
About the Role We are seeking a board-certified Gastroenterologist to serve as a Principal Investigator (PI) or Sub-Investigator (Sub-I) in Phase I IV clinical trials. The physician will provide medical oversight, ensure protocol compliance, monitor participant safety, and collaborate with research staff and sponsors to advance high-quality clinical research.
Key Responsibilities
Serve as PI or Sub-I in gastroenterology and multi-therapeutic clinical trials
Conduct medical screenings, assessments, and physical examinations
Ensure patient safety and compliance with study protocols, ICH-GCP, and regulatory standards
Document patient data, adverse events, and study outcomes accurately
Collaborate with study coordinators, nurses, monitors, CROs, and sponsors
Participate in site initiation visits, monitoring visits, audits, and investigator meetings
Contribute to protocol feasibility reviews, study design input, and recruitment strategies
Qualifications
MD or DO with an active Arizona medical license
Board certification in Gastroenterology
DEA license and BLS / ACLS certification
Clinical research experience preferred (training available for motivated candidates)
Strong communication, organizational, and documentation skills
Commitment to ethical research practices and patient-centered care
Benefits
Flexible part-time schedule
Opportunity to contribute to groundbreaking gastroenterology research
Professional growth in clinical research
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Location: Scottsdale, AZ
Schedule: Part-Time (0 8 hours / week)
Start Date: Within 0 6 months
About the Role We are seeking a board-certified Gastroenterologist to serve as a Principal Investigator (PI) or Sub-Investigator (Sub-I) in Phase I IV clinical trials. The physician will provide medical oversight, ensure protocol compliance, monitor participant safety, and collaborate with research staff and sponsors to advance high-quality clinical research.
Key Responsibilities
Serve as PI or Sub-I in gastroenterology and multi-therapeutic clinical trials
Conduct medical screenings, assessments, and physical examinations
Ensure patient safety and compliance with study protocols, ICH-GCP, and regulatory standards
Document patient data, adverse events, and study outcomes accurately
Collaborate with study coordinators, nurses, monitors, CROs, and sponsors
Participate in site initiation visits, monitoring visits, audits, and investigator meetings
Contribute to protocol feasibility reviews, study design input, and recruitment strategies
Qualifications
MD or DO with an active Arizona medical license
Board certification in Gastroenterology
DEA license and BLS / ACLS certification
Clinical research experience preferred (training available for motivated candidates)
Strong communication, organizational, and documentation skills
Commitment to ethical research practices and patient-centered care
Benefits
Flexible part-time schedule
Opportunity to contribute to groundbreaking gastroenterology research
Professional growth in clinical research
#J-18808-Ljbffr