Job Summary
This position is for a Clinical Research Associate specializing in Early Clinical Development, focusing on supporting Phase I trials across various locations in the U.S. The role primarily involves ensuring the integrity and organization of critical trial documentation within the Trial Master File and Investigator Site File systems.
Responsibilities
- Support Phase I early clinical development trials by managing essential trial documentation.
- Maintain the organization and accuracy of the Trial Master File and Investigator Site File systems.
- Coordinate with diverse teams across multiple U.S. locations to facilitate trial operations.
Qualifications
- A Bachelor’s degree in a relevant field.
- Experience or familiarity with clinical trial processes and documentation requirements.
- Strong organizational skills and attention to detail.
IQVIA 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.
