Protouch Staffing
Rheumatologist (Clinical Trial Physician)
Protouch Staffing, San Jose, California, United States, 95199
Rheumatologist (Clinical Trial Physician) - San Jose, CA
Job Type: Part-Time
Shift: Day
Position Summary:
We are seeking a board-certified Rheumatologist to serve as a Principal Investigator (PI) or Sub-Investigator (Sub-I) in our current and upcoming clinical trials. The Rheumatologist will oversee study participants, ensure protocol compliance, monitor patient safety, and collaborate with the research team to maintain high-quality trial execution.
Key Responsibilities:
Serve as PI or Sub-I in assigned clinical trials. Conduct medical evaluations and assess participant eligibility. Monitor patient safety, adverse events, and treatment outcomes. Review and sign study-related documentation per protocol and regulations. Collaborate with study coordinators, nurses, and other research staff. Attend protocol training and ensure adherence to Good Clinical Practice (GCP). Qualifications:
MD or DO with an active California medical license . Board-certified in Rheumatology . Interest in clinical research (prior experience preferred; training provided if needed). Strong communication, teamwork, and organizational skills. Compensation & Benefits:
$100-$200 per hour (depending on study complexity). Flexible schedule: 0-8 hours/week. Professional growth opportunities in clinical research. Contribute to advancing rheumatology treatments and improving patient outcomes.
Position Summary:
We are seeking a board-certified Rheumatologist to serve as a Principal Investigator (PI) or Sub-Investigator (Sub-I) in our current and upcoming clinical trials. The Rheumatologist will oversee study participants, ensure protocol compliance, monitor patient safety, and collaborate with the research team to maintain high-quality trial execution.
Key Responsibilities:
Serve as PI or Sub-I in assigned clinical trials. Conduct medical evaluations and assess participant eligibility. Monitor patient safety, adverse events, and treatment outcomes. Review and sign study-related documentation per protocol and regulations. Collaborate with study coordinators, nurses, and other research staff. Attend protocol training and ensure adherence to Good Clinical Practice (GCP). Qualifications:
MD or DO with an active California medical license . Board-certified in Rheumatology . Interest in clinical research (prior experience preferred; training provided if needed). Strong communication, teamwork, and organizational skills. Compensation & Benefits:
$100-$200 per hour (depending on study complexity). Flexible schedule: 0-8 hours/week. Professional growth opportunities in clinical research. Contribute to advancing rheumatology treatments and improving patient outcomes.