Protouch Staffing
Job Title:
Clinical Research Rheumatologist 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 Rheumatologist to serve as a Principal Investigator (PI) or Sub-Investigator (Sub-I) in Phase I-IV clinical trials. The physician will oversee study participants, ensure protocol compliance, monitor patient safety, and collaborate with research staff and sponsors to deliver high-quality clinical research. Key Responsibilities Serve as PI or Sub-I in rheumatology and multi-therapeutic clinical trials
Conduct medical screenings, assessments, and physical exams
Provide clinical oversight and ensure adherence to protocols, ICH-GCP, and regulatory standards
Document subject data, adverse events, and study outcomes accurately
Collaborate with study coordinators, nurses, CROs, and sponsors
Participate in site visits, audits, and investigator meetings
Qualifications MD or DO with an active Arizona medical license
Board-certified in Rheumatology
DEA license and BLS/ACLS certification
Clinical research experience preferred (training available)
Strong communication and organizational skills
Benefits Flexible part-time schedule
Opportunity to contribute to advancing rheumatology treatments
Professional growth in clinical research
If you're interested, please let me know a convenient time to chat, or feel free to contact me directly at or via email at .
Clinical Research Rheumatologist 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 Rheumatologist to serve as a Principal Investigator (PI) or Sub-Investigator (Sub-I) in Phase I-IV clinical trials. The physician will oversee study participants, ensure protocol compliance, monitor patient safety, and collaborate with research staff and sponsors to deliver high-quality clinical research. Key Responsibilities Serve as PI or Sub-I in rheumatology and multi-therapeutic clinical trials
Conduct medical screenings, assessments, and physical exams
Provide clinical oversight and ensure adherence to protocols, ICH-GCP, and regulatory standards
Document subject data, adverse events, and study outcomes accurately
Collaborate with study coordinators, nurses, CROs, and sponsors
Participate in site visits, audits, and investigator meetings
Qualifications MD or DO with an active Arizona medical license
Board-certified in Rheumatology
DEA license and BLS/ACLS certification
Clinical research experience preferred (training available)
Strong communication and organizational skills
Benefits Flexible part-time schedule
Opportunity to contribute to advancing rheumatology treatments
Professional growth in clinical research
If you're interested, please let me know a convenient time to chat, or feel free to contact me directly at or via email at .