Gastrointestinal GI -Clinical Research

Benefits

Qualifications

• •with an active, unrestricted Texas medical license
• •Board-certified in any specialty (Gastroenterology, Cardiology, Dermatology, Pain Management/PMNR, Nephrology)
• •Valid DEA license and current BLS/ACLS certification
• •Proficiency with EHR systems and clinical trial platforms (EDC, CTMS)
• •Strong communication and interpersonal skills with a collaborative mindset
• •Commitment to ethical, patient-centered research
• •Gain or expand experience in clinical research
• •4 more items(s)

Responsibilities

• •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
• •Key Responsibilities 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
• •8 more items(s)