Study Start Up Specialist

ICON Clinical Research, LP

Shanghai, China
Conducting site qualification visits
Ensuring protocol compliance
Data integrity and patient safety
As a Clinical Research Associate (SSU) 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 Associate (SSU) 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 range of additional benefits designed to be competitive within each country and 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 we are dedicated to providing an inclusive and accessible environment for all candidates.

Matching Summary

As a Clinical Research Associate (SSU) 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

  • Conducting site qualification visits
  • Ensuring protocol compliance
  • Data integrity and patient safety
  • Collaborating with investigators and site staff
  • Data review and query resolution
  • Study documentation preparation and review

Nice-to-have

  • Fostering an inclusive environment
  • Driving innovation and excellence
  • Shaping the future of clinical development
  • Nurturing talent and rewarding performance

Key Requirements

  • Minimum of 2 years of experience as a Clinical Research Associate
  • In-depth knowledge of clinical trial processes
  • Knowledge of regulations and ICH-GCP guidelines
  • Bachelor's degree in a scientific or healthcare-related field

Work Rights

Not specified

Tailored Resume

Cover Letter