Clinical Trial Coord Ii

PPD (Thermo Fisher) UK

Shanghai, China
Clinical trial document management
Site activation coordination
Audit readiness support
Join a global team supporting top pharmaceutical companies and biotechs across thousands of clinical trials worldwide

Job Summary

  • Join a global team supporting top pharmaceutical companies and biotechs across thousands of clinical trials worldwide.
  • You will provide critical administrative and technical support to ensure timely site activations and audit readiness.
  • The role offers opportunities to contribute to global feasibility processes and to train new staff members.

Matching Summary

Join a global team supporting top pharmaceutical companies and biotechs across thousands of clinical trials worldwide.

Skills & Requirements

Must-have

  • Clinical trial document management
  • Site activation coordination
  • Audit readiness support
  • Use of Activate and eTMF systems
  • Regulatory compliance knowledge
  • Project task coordination
  • Data analysis and reconciliation

Nice-to-have

  • Training new personnel
  • Local site knowledge utilization
  • Risk management and escalation
  • Strong customer focus
  • Effective communication skills
  • Independent and team work capability
  • Multilingual skills

Key Requirements

  • High/Secondary school diploma or equivalent
  • Bachelor's degree preferred
  • 0 to 1 year relevant experience
  • Knowledge of ICH GCP and regulatory guidelines
  • Proficiency in MS Office and clinical trial databases
  • Ability to complete clinical training program

Work Rights

Not specified

Tailored Resume

Cover Letter