Clinical Study Manager

ICON

San Antonio, TX, United States
Clinical trial planning and execution
Regulatory compliance management
Project timeline management
As a Clinical Study Manager at ICON, you will play a pivotal role in overseeing the planning, execution, and delivery of clinical trials, contributing to the advancement of innovative treatments and therapies

Job Summary

  • As a Clinical Study Manager at ICON, you will play a pivotal role in overseeing the planning, execution, and delivery of clinical trials, contributing to the advancement of innovative treatments and therapies.
  • ICON offers a range of additional benefits designed to be competitive within each country and are focused on well-being and work life balance opportunities for you and your family.
  • At ICON, inclusion & belonging are fundamental to our culture and values, and the company is committed to providing a workplace free of discrimination and harassment.

Matching Summary

As a Clinical Study Manager at ICON, you will play a pivotal role in overseeing the planning, execution, and delivery of clinical trials, contributing to the advancement of innovative treatments and therapies.

Skills & Requirements

Must-have

  • clinical trial planning and execution
  • regulatory compliance management
  • project timeline management
  • cross-functional team collaboration
  • study budget and resource management
  • data integrity and quality assurance

Nice-to-have

  • problem-solving and communication skills
  • inclusive and diverse work culture
  • work-life balance focus

Key Requirements

  • Bachelor's degree in scientific discipline
  • proven clinical study management experience
  • strong understanding of drug development process
  • knowledge of regulatory requirements

Work Rights

Not specified

Tailored Resume

Cover Letter