Senior Clinical Research Associate - West Coast - Fsp

Parexel

Remote
Fully remote
Clinical trial methodologies
Site monitoring experience
Gcp compliance
The Senior Clinical Research Associate is responsible for site management and monitoring of clinical trials

Job Summary

  • The Senior Clinical Research Associate is responsible for site management and monitoring of clinical trials.
  • This role ensures patient safety and quality study execution in accordance with applicable laws and standards.
  • At Parexel, we are committed to improving the world's health and making a difference.

Matching Summary

The Senior Clinical Research Associate is responsible for site management and monitoring of clinical trials.

Skills & Requirements

Must-have

  • Clinical trial methodologies
  • Site monitoring experience
  • GCP compliance

Nice-to-have

  • Oncology therapeutic experience
  • Strong communication skills
  • Team collaboration

Key Requirements

  • Minimum 3 years clinical research experience
  • Bachelor’s degree in life sciences
  • Fluency in English and local language

Work Rights

Not specified

Tailored Resume

Cover Letter