Associate Clinical Operations Manager

Philips UK

Shanghai, China
Hybrid
Clinical research studies management
Study protocol training
Regulatory statutes adherence
You are responsible for the management and monitoring of clinical research studies involving human subjects from its inception to close-out according to budget and timelines

Job Summary

  • You are responsible for the management and monitoring of clinical research studies involving human subjects from its inception to close-out according to budget and timelines.
  • Ensures that assigned site staff are appropriately trained to the study protocol and to ensure study and data integrity in support of a broader Clinical Evidence Strategy.
  • A path towards your most rewarding career with high level of autonomy.

Matching Summary

You are responsible for the management and monitoring of clinical research studies involving human subjects from its inception to close-out according to budget and timelines.

Skills & Requirements

Must-have

  • Clinical research studies management
  • Study protocol training
  • Regulatory statutes adherence
  • Stakeholder interface
  • Investigator qualification and training
  • Clinical study monitoring

Nice-to-have

  • Customer-first attitude
  • Meaningful solutions creation
  • Innovative environment exploration
  • Hybrid work flexibility
  • Impactful collaboration

Key Requirements

  • BS/BA in scientific or relevant discipline
  • GCP Certification of NMPA
  • Clinical Study monitoring and management training
  • Minimum of 3+ years experience
  • Site assessment/monitoring experience

Work Rights

Not specified

Tailored Resume

Cover Letter