Clinical Research Gastroenterologist - San Antonio, TX
Job Type : Part-time (0-8 hours per week, flexible schedule)
Start Date : Within 0-6 months
Responsibilities :
- Serve as Principal Investigator (PI) or Sub-Investigator (Sub-I) across Phase I-IV 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.
Qualifications :
M.D. or D.O. with an active, unrestricted Texas medical license.Board-certified in Gastro enterologyValid DEA license and current BLS / ACLS certification.Prior clinical research experience preferred (training available).Proficiency with EHR systems and clinical trial platforms (EDC, CTMS).Compensation & Benefits :
Competitive hourly rate : $100 - $250 based on specialty and 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.by Jobble