Trainee Cra

Thermo Fisher Scientific UK

Guangdong, China
Fully remote
Ich gcp understanding
Crg procedural documents
Remote monitoring support
As a Trainee Clinical Research Associate, you'll provide support with site preparedness, logistical support to the monitoring process, and assist with assigned tasks for site management and remote monitoring in accordance with SOPs and regulatory guidelines

Job Summary

  • As a Trainee Clinical Research Associate, you'll provide support with site preparedness, logistical support to the monitoring process, and assist with assigned tasks for site management and remote monitoring in accordance with SOPs and regulatory guidelines.
  • You will complete study and site management activities as defined in the task matrix, complete and document study-specific training, and orient and train on any CRG/study-specific systems.
  • Responsibilities include verifying document collection and RCR submission status, supporting site staff with vendor qualification, coordinating study/site supply management, and performing reconciliation tasks on assigned trials.

Matching Summary

As a Trainee Clinical Research Associate, you'll provide support with site preparedness, logistical support to the monitoring process, and assist with assigned tasks for site management and remote monitoring in accordance with SOPs and regulatory guidelines.

Skills & Requirements

Must-have

  • ICH GCP understanding
  • CRG procedural documents
  • remote monitoring support
  • site management tasks
  • Crucial Document collection
  • vendor qualification process support

Nice-to-have

  • strong attention to detail
  • proven flexibility and adaptability
  • critical thinking skills
  • customer service skills
  • team or independent work

Key Requirements

  • Bachelor's degree or equivalent
  • 0 to 2 years relevant experience
  • Basic medical/therapeutic area knowledge
  • Proficient digital literacy with MS Office

Work Rights

Not specified

Tailored Resume

Cover Letter