Protouch Staffing
Part-Time Clinical Research Endocrinologist
Location: Webster, TX
Schedule: Flexible | 0-8 hours/week
Start Date: Within 0-6 months
We are seeking a Board-Certified Endocrinologist to join our clinical research site as a Principal Investigator (PI) or Sub-Investigator (Sub-I) . This role offers a unique opportunity to contribute to innovative clinical trials in endocrinology and related therapeutic areas, while enjoying the benefits of a highly flexible, part-time schedule . Key Responsibilities
Serve as PI or Sub-I across Phase I-IV clinical trials Conduct screenings, endocrine assessments, and physical exams Ensure participant safety and protocol compliance (ICH-GCP, FDA, IRB) Collaborate with research staff, coordinators, and nurses for trial execution Document patient visits, monitor AEs/SAEs, and maintain compliance with EHR/EDC systems Provide endocrinology expertise during feasibility reviews and study design discussions Engage with sponsors, CROs, and monitors to support trial success Qualifications M.D. or D.O. with an active, unrestricted Texas license Board-certified in Endocrinology (other specialties accepted except Psychiatry, Gastroenterology, Internal Medicine, Cardiology) Valid DEA license + current BLS/ACLS certification Clinical research experience preferred (training provided) Strong communication and teamwork skills What We Offer Flexible part-time schedule (0-8 hrs/week) - ideal for supplemental income or work-life balance Opportunity to expand your experience in clinical research Be part of advancing innovative therapies in endocrinology
Interested? Contact Kamal at (469) 210-0176 or kamal.deen@protouchstaffing.com
We are seeking a Board-Certified Endocrinologist to join our clinical research site as a Principal Investigator (PI) or Sub-Investigator (Sub-I) . This role offers a unique opportunity to contribute to innovative clinical trials in endocrinology and related therapeutic areas, while enjoying the benefits of a highly flexible, part-time schedule . Key Responsibilities
Serve as PI or Sub-I across Phase I-IV clinical trials Conduct screenings, endocrine assessments, and physical exams Ensure participant safety and protocol compliance (ICH-GCP, FDA, IRB) Collaborate with research staff, coordinators, and nurses for trial execution Document patient visits, monitor AEs/SAEs, and maintain compliance with EHR/EDC systems Provide endocrinology expertise during feasibility reviews and study design discussions Engage with sponsors, CROs, and monitors to support trial success Qualifications M.D. or D.O. with an active, unrestricted Texas license Board-certified in Endocrinology (other specialties accepted except Psychiatry, Gastroenterology, Internal Medicine, Cardiology) Valid DEA license + current BLS/ACLS certification Clinical research experience preferred (training provided) Strong communication and teamwork skills What We Offer Flexible part-time schedule (0-8 hrs/week) - ideal for supplemental income or work-life balance Opportunity to expand your experience in clinical research Be part of advancing innovative therapies in endocrinology
Interested? Contact Kamal at (469) 210-0176 or kamal.deen@protouchstaffing.com