Base: $25.00-$39.00 ph; bonus/equity: not specifie...
Onsite
Edc data entry and query resolution
Review patient charts and records
Participant screening and recruitment
The Research Assistant plays a critical role in supporting clinical trial activities in accordance with GCP, IRB, and all applicable regulatory requirements
Job Summary
The Research Assistant plays a critical role in supporting clinical trial activities in accordance with GCP, IRB, and all applicable regulatory requirements.
Key responsibilities include performing EDC data entry and query resolution, reviewing patient charts, assisting in participant recruitment, and managing participant scheduling.
IQVIA is a global leader in advanced analytics, technology solutions, and clinical research services, dedicated to driving healthcare forward.
Matching Summary
The Research Assistant plays a critical role in supporting clinical trial activities in accordance with GCP, IRB, and all applicable regulatory requirements.
Salary
Base: $25.00-$39.00 per hour; Bonus/Equity: Not specified; Benefits: Not specified
Skills & Requirements
Must-have
EDC data entry and query resolution
Review patient charts and records
Participant screening and recruitment
Participant visit scheduling
Adherence to GCP and regulatory guidelines
Nice-to-have
Strong attention to detail
Excellent communication skills
Ability to collaborate effectively
Key Requirements
Associate's degree or equivalent experience
1 year clinical research experience preferred
Working knowledge of clinical trials and GCP principles
Familiarity with cardiovascular studies preferred
Experience with EDC entry and query resolution
Experience with prescreening referrals
Experience with chart review from site databases
Experience with visit scheduling and reminders
Experience maintaining study supplies and regulatory binders