Research Intern - Anesthesiology and PeriOperative Medicine
- Requisition #: 600658-202505301757
- Department: Anesthesiology and PeriOp Med-Res
- Location: Houston, TX
- Posted Date: 5/30/2025
The program is designed to learn about the execution and management of an ongoing clinical trial focused on the impact of anesthetics on recovery after surgery. This internship provides hands-on experience in clinical research, offering exposure to the design, implementation, and monitoring of clinical studies in a regulated environment.
Key Responsibilities:
• Assist with data collection, entry, and quality control for clinical trial participants.
• Support the preparation and maintenance of study documentation, including informed consent forms, case report forms, and regulatory binders.
• Participate in patient recruitment and follow-up activities under supervision.
• Help coordinate communication between research staff, anesthesiologists, CRNAs and AAs, and study sponsors.
• Attend team meetings and contribute to discussions on study progress and challenges.
• Conduct literature reviews and assist in preparing reports or presentations related to the study.
LEARNING OBJECTIVES
• Gain a foundational understanding of clinical trial phases and regulatory requirements.
• Develop skills in data management, patient interaction, and research ethics.
• Learn how to work collaboratively in a multidisciplinary research environment.
ELIGIBILITY REQUIREMENTS
Bachelor's degree
POSITION INFORMATION
06/30/2025
Key Responsibilities:
• Assist with data collection, entry, and quality control for clinical trial participants.
• Support the preparation and maintenance of study documentation, including informed consent forms, case report forms, and regulatory binders.
• Participate in patient recruitment and follow-up activities under supervision.
• Help coordinate communication between research staff, anesthesiologists, CRNAs and AAs, and study sponsors.
• Attend team meetings and contribute to discussions on study progress and challenges.
• Conduct literature reviews and assist in preparing reports or presentations related to the study.
LEARNING OBJECTIVES
• Gain a foundational understanding of clinical trial phases and regulatory requirements.
• Develop skills in data management, patient interaction, and research ethics.
• Learn how to work collaboratively in a multidisciplinary research environment.
ELIGIBILITY REQUIREMENTS
Bachelor's degree
POSITION INFORMATION
