(senior) Clinical Research Associate - Fsp

Parexel

Multiple Locations
Fully remote
Clinical trial monitoring experience
Knowledge of ich/gcp regulations
Experience in oncology preferred
At Parexel, we share a goal to improve the world's health through clinical trials and regulatory consulting. The role involves oversight of clinical trials ensuring compliance with laws and quality standards. You will collaborate with study teams and investigator sites to facilitate successful trial delivery

Job Summary

  • At Parexel, we share a goal to improve the world's health through clinical trials and regulatory consulting. The role involves oversight of clinical trials ensuring compliance with laws and quality standards. You will collaborate with study teams and investigator sites to facilitate successful trial delivery.

Matching Summary

At Parexel, we share a goal to improve the world's health through clinical trials and regulatory consulting. The role involves oversight of clinical trials ensuring compliance with laws and quality standards. You will collaborate with study teams and investigator sites to facilitate successful trial delivery.

Skills & Requirements

Must-have

  • Clinical trial monitoring experience
  • Knowledge of ICH/GCP regulations
  • Experience in Oncology preferred

Nice-to-have

  • Strong communication skills
  • Ability to work in a matrix team
  • Empathetic approach to patient care

Key Requirements

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

Work Rights

Not specified

Tailored Resume

Cover Letter