Bachelor’s degree in a relevant field (e.g., healthcare, life sciences) or International Medical Graduate. Collaborate with healthcare professionals to support patient care within the study's scope.
Numbers & Facts
Location
Desoto, Texas
Description
Oversee and manage clinical research studies from inception to conclusion
Collect, document, and maintain study data in compliance with protocol requirements
Conduct patient monitoring, including assessments of vital signs
Supervise and train research personnel on study protocols and procedures
Ensure compliance with FDA regulations and guidelines throughout the research process
Review and maintain documentation about the research studies
Collaborate with healthcare professionals to support patient care within the study's scope
Assist in the collection, analysis, and interpretation of data for research projects
Requirements
Bachelor’s degree in a relevant field (e.g., healthcare, life sciences) or International Medical Graduate
Previous experience in clinical research or a related field
Knowledge of medical terminology and clinical trial processes
Familiarity with data management practices and electronic data capture systems
Strong organizational skills with a high attention to detail
Ability to work independently and collaboratively within a multidisciplinary team
Excellent communication and interpersonal skills for effective collaboration
Understanding of ethical considerations in clinical research