IQVIA
This role involves performing daily administrative activities to support Clinical Research Associates and Regulatory teams in delivering accurate Trial Master Files. Key duties include maintaining clinical documents, managing trial supplies, tracking Case Report Forms, and assisting with site visits after training. The position requires strong organizational skills and knowledge of clinical research regulatory requirements.
IQVIA empowers life sciences organizations to accelerate innovation, improve patient outcomes, and bring treatments to market faster through advanced analytics and technology.
Headquarters
San Francisco, CA
Company Size
201-500 employees
Founded
2018
Industry
Technology
Glassdoor Rating
4.2 / 5
Sarah Johnson
Chief Executive Officer
Michael Chen
Chief Technology Officer
Emily Williams
VP of Engineering
David Rodriguez
VP of Product
Jessica Thompson
Chief Financial Officer
Andrew Park
VP of Sales
View leadership team, funding history,
and employee contacts for IQVIA.
IQVIA didn’t post a salary, so this is our estimate from similar listings.
4% above the average for this role