ProTouch Staffing
Endocrinology Physician
ProTouch Staffing, Charter Township of Clinton, Michigan, United States
Overview
Endocrinologist (Clinical Trial Physician) role in Clinton Township, CA, 0-8 hours per week, start date within 0-6 months. We are seeking a board-certified Endocrinologist to serve as Principal Investigator (PI) or Sub-Investigator (Sub-I) in our current and upcoming clinical trials. The Endocrinologist will oversee study participants, ensure protocol compliance, monitor patient safety, and collaborate with research staff to maintain high-quality trial execution. Responsibilities
Serve as PI or Sub-I in clinical trials. Conduct medical evaluations and assess participant eligibility. Monitor patient safety, adverse events, and treatment outcomes. Review and sign study-related documentation according to protocol and regulations. Collaborate with study coordinators, nurses, and research staff. Attend protocol training and maintain adherence to Good Clinical Practice (GCP). Qualifications
MD or DO with an active medical license in California. Board-certified in Endocrinology. Interest in clinical research (prior experience preferred; training provided if needed). Strong communication and organizational skills. Compensation & Benefits
Flexible schedule (0-8 hours / week). Professional growth in clinical research. Opportunity to contribute to advancing endocrinology treatments.
#J-18808-Ljbffr
Endocrinologist (Clinical Trial Physician) role in Clinton Township, CA, 0-8 hours per week, start date within 0-6 months. We are seeking a board-certified Endocrinologist to serve as Principal Investigator (PI) or Sub-Investigator (Sub-I) in our current and upcoming clinical trials. The Endocrinologist will oversee study participants, ensure protocol compliance, monitor patient safety, and collaborate with research staff to maintain high-quality trial execution. Responsibilities
Serve as PI or Sub-I in clinical trials. Conduct medical evaluations and assess participant eligibility. Monitor patient safety, adverse events, and treatment outcomes. Review and sign study-related documentation according to protocol and regulations. Collaborate with study coordinators, nurses, and research staff. Attend protocol training and maintain adherence to Good Clinical Practice (GCP). Qualifications
MD or DO with an active medical license in California. Board-certified in Endocrinology. Interest in clinical research (prior experience preferred; training provided if needed). Strong communication and organizational skills. Compensation & Benefits
Flexible schedule (0-8 hours / week). Professional growth in clinical research. Opportunity to contribute to advancing endocrinology treatments.
#J-18808-Ljbffr