**Job Title: Clinical Trial Assistant**
In this position, you will assist with the initiation of clinical trials, which involves gathering regulatory documents, conducting site qualification assessments, and preparing study files. Additionally, you will be responsible for maintaining the Trial Master File and providing updates on trial progress to management. A bachelor’s degree in life sciences is highly desirable, alongside a minimum of two years of experience in a Clinical Research Coordinator or Clinical Trial Assistant role. Candidates should possess a solid understanding of Good Clinical Practice (GCP) and regulatory matters, and be willing to travel 30-40% of the time.
Abbott Laboratories provides equal employment opportunities to all employees and applicants for employment and prohibits discrimination and harassment of any type without regard to race, color, religion, age, sex, national origin, disability status, genetics, protected veteran status, sexual orientation, gender identity or expression, or any other characteristic protected by federal, state or local laws.
