Clinical Research Rheumatologist - 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 Rheumatology
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).
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.
