Protouch Staffing
Clinical Trial Physician (Specialized Fields)
Protouch Staffing, Pomona, California, United States, 91768
Endocrinologist (Clinical Trial Physician)
Location: , Pomona, CA Commitment: 0-8 hours/week Start Date: Within 0-6 months Position Summary
We are seeking board-certified physicians in the following specialties to serve as Principal or Sub-Investigators in our ongoing and upcoming clinical trials:
Endocrinologist/Obesity Medicine Physicians will oversee study participants, ensure protocol compliance, monitor patient safety, and collaborate with research teams to deliver high-quality trial outcomes. Key Responsibilities
Serve as Sub-Investigator or Principal Investigator Conduct medical evaluations and assess participant eligibility Monitor patient safety, adverse events, and outcomes Review and sign study-related documentation Collaborate with research coordinators and staff Maintain compliance with Good Clinical Practice (GCP) Qualifications MD or DO with an active state medical license Board-certified in one of the listed specialties Clinical research interest (experience preferred) Strong communication and organizational skills Compensation & Benefits Flexible scheduling (0-8 hrs/week) Research training and professional growth opportunities Impactful contribution to advancing medical science
For more details: Contact: 469-991-3805 (or) Email me at: winston.harper@protouchstaffing.com
Location: , Pomona, CA Commitment: 0-8 hours/week Start Date: Within 0-6 months Position Summary
We are seeking board-certified physicians in the following specialties to serve as Principal or Sub-Investigators in our ongoing and upcoming clinical trials:
Endocrinologist/Obesity Medicine Physicians will oversee study participants, ensure protocol compliance, monitor patient safety, and collaborate with research teams to deliver high-quality trial outcomes. Key Responsibilities
Serve as Sub-Investigator or Principal Investigator Conduct medical evaluations and assess participant eligibility Monitor patient safety, adverse events, and outcomes Review and sign study-related documentation Collaborate with research coordinators and staff Maintain compliance with Good Clinical Practice (GCP) Qualifications MD or DO with an active state medical license Board-certified in one of the listed specialties Clinical research interest (experience preferred) Strong communication and organizational skills Compensation & Benefits Flexible scheduling (0-8 hrs/week) Research training and professional growth opportunities Impactful contribution to advancing medical science
For more details: Contact: 469-991-3805 (or) Email me at: winston.harper@protouchstaffing.com