We are seeking board-certified Endocrinologist to join our clinical research site.

This part-time position offers physicians the opportunity to contribute to groundbreaking medical research while maintaining a flexible schedule. You will serve as a Principal Investigator (PI) or Sub-Investigator (Sub-I), overseeing clinical trial activities and ensuring the highest standards of patient safety and protocol compliance across Phase I-IV studies.

• Serve as PI or Sub-I across clinical trials in diverse therapeutic areas.

• Conduct medical screenings, specialty assessments, and physical examinations.

• Ensure participant safety and protocol adherence in compliance with ICH-GCP, FDA, and regulatory standards.

• Collaborate with coordinators, nurses, and research staff for accurate documentation and trial execution.

• Document patient interactions, monitor adverse events (AEs/SAEs), and maintain compliance with EHR/EDC systems.

• Engage with sponsors, CROs, monitors, and IRBs to support trial success.

• Participate in site initiation visits, monitoring visits, and audits.

• Provide medical expertise during feasibility reviews, recruitment strategies, and study design discussions.

• Stay updated on clinical research regulations and advances in investigational therapies.

• M.D. or D.O. with an active, unrestricted Texas medical license.
• Required Candidates who have their Own Practice.
• Board-certified in Endocrinology
  
• Valid DEA license and current BLS/ACLS certification.
• Prior clinical research experience preferred (training available).
• Proficiency with EHR systems and clinical trial platforms (EDC, CTMS).
• Commitment to ethical, patient-centered research.

• Compensation & Benefits

• Competitive hourly rate: $100 - $250 based on experience.

• Highly flexible, part-time schedule (ideal for supplemental income or work-life balance).

• Gain or expand experience in clinical research.

• Contribute to the advancement of medical innovation and patient care.