Protouch Staffing
Rheumatologist (Clinical Trial Physician)
Protouch Staffing, San Jose, California, United States, 95199
Overview
Rheumatologist (Clinical Trial Physician) f San Jose, CA. Part-Time. Day shift. 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. 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.
#J-18808-Ljbffr
Rheumatologist (Clinical Trial Physician) f San Jose, CA. Part-Time. Day shift. 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. 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.
#J-18808-Ljbffr