Clinical Study Coordinator

ICON

San Antonio, TX, United States
Clinical research study coordination
Participant recruitment and enrollment
Clinical trial data management
As a Clinical Research Coordinator at ICON, you will play a pivotal role in designing and analyzing clinical trials, interpreting complex medical data, and contributing to the advancement of innovative treatments and therapies

Job Summary

  • As a Clinical Research Coordinator at ICON, you will play a pivotal role in designing and analyzing clinical trials, interpreting complex medical data, and contributing to the advancement of innovative treatments and therapies.
  • ICON offers a diverse and inclusive culture that rewards high performance and nurtures talent with a range of benefits focused on well-being and work-life balance.
  • The role requires facilitating coordination and execution of clinical research studies, ensuring compliance with protocols and regulatory requirements, and managing study-related documentation.

Matching Summary

As a Clinical Research Coordinator at ICON, you will play a pivotal role in designing and analyzing clinical trials, interpreting complex medical data, and contributing to the advancement of innovative treatments and therapies.

Skills & Requirements

Must-have

  • clinical research study coordination
  • participant recruitment and enrollment
  • clinical trial data management
  • regulatory compliance with FDA/EMA
  • ICH-GCP guidelines adherence
  • documentation of adverse events

Nice-to-have

  • collaboration with principal investigators
  • support and guidance to study participants
  • strong organizational and communication skills
  • team environment adaptability
  • detail-oriented multitasking

Key Requirements

  • Bachelor's degree in scientific or healthcare field
  • experience as Clinical Research Coordinator preferred
  • knowledge of FDA/EMA regulations
  • understanding of ICH-GCP guidelines
  • HIPAA requirements knowledge

Work Rights

Not specified

Tailored Resume

Cover Letter