Clinical Trial Assistant (Clinical Research)

Location: Hybrid in Wilmington, Delaware, United States

Salary: $35,800–$123,000 annualized base pay, depending on qualifications, location, and schedule.

Company

IQVIA provides clinical research services, commercial insights, and healthcare intelligence for the life sciences and healthcare industries.

What you will do

• Support Clinical Research Associates and Regulatory and Start-Up teams with maintaining clinical documents and systems, including Trial Master Files.
• Prepare, handle, distribute, file, and archive clinical documentation and reports according to project requirements and standard operating procedures.
• Review study files for completeness and track site compliance and performance within project timelines.
• Support the preparation and tracking of clinical trial supplies and related documentation.
• Track Case Report Forms, queries, and clinical data flow while coordinating project communications.
• Accompany CRAs on site visits after completing the required training to support clinical monitoring activities.

Requirements

• Bachelor’s degree or an equivalent combination of education, training, and experience.
• Three years of administrative support experience.
• Working knowledge of Microsoft Word, Excel, and PowerPoint.
• Good command of English, with strong written and verbal communication skills.
• Effective time-management, organizational, and relationship-building skills.
• Awareness of Good Clinical Practice and International Conference on Harmonization guidelines, as well as applicable protocol requirements.

Culture & Benefits

• Full-time employment with a potential annualized base pay range of $35,800–$123,000.
• Health, welfare, and other benefits may be provided.
• Incentive plans, bonuses, or other compensation may be available depending on the position.
• Equal opportunity employment and a hiring process focused on accurate, complete candidate information.