Site Research Assistant - Ponce, Puerto Rico

IQVIA Inc

Ponce, Puerto Rico
Base: $0.00 - $86,000.00 annualized; bonus/equity:...
On-site, part-time (20 hours per week)
Edc data entry and query resolution
Patient chart review from site databases
Spanish bilingual proficiency required
IQVIA Inc is seeking a Site Research Assistant in Ponce, Puerto Rico, for a part-time, on-site role focused on supporting clinical trial activities. The ideal candidate should have experience in clinical research, particularly in cardiovascular studies, and possess strong attention to detail, organizational skills, and bilingual proficiency in Spanish

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, reviewing patient charts, assisting in screening and recruiting participants, and ensuring informed consent adherence.
  • IQVIA is a global leader dedicated to driving healthcare forward by partnering with leading pharmaceutical and biotechnology companies to improve patient outcomes.

Matching Summary

Match Score: 85

IQVIA Inc is seeking a Site Research Assistant in Ponce, Puerto Rico, for a part-time, on-site role focused on supporting clinical trial activities. The ideal candidate should have experience in clinical research, particularly in cardiovascular studies, and possess strong attention to detail, organizational skills, and bilingual proficiency in Spanish.

Salary

Base: $0.00 - $86,000.00 annualized; Bonus/Equity: Not specified; Benefits: Health and welfare benefits offered

Skills & Requirements

Must-have

  • EDC data entry and query resolution
  • Patient chart review from site databases
  • Spanish bilingual proficiency required

Nice-to-have

  • Experience in cardiovascular studies
  • Strong attention to detail
  • Ability to prioritize in fast-paced environment

Key Requirements

  • Associate degree preferred or equivalent experience
  • 1+ years of experience in clinical research setting
  • Spanish bilingual language requirement
  • Not eligible for sponsorship

Work Rights

US work authorization required (sponsorship not available)

Tailored Resume

Cover Letter