Data Compliance Specialist

Thermo Fisher Scientific UK

Unknown, Unknown, United Kingdom
**
Clinical trial experience essential
Ecrf data entry and accuracy
Ich gcp regulatory knowledge
** Thermo Fisher Scientific UK is seeking a Data Compliance Specialist to ensure accurate documentation and compliance within clinical trials. The role involves managing data entry in electronic case report forms (eCRF), conducting quality checks, and acting as a liaison between sponsors and site representatives. **

Job Summary

  • The role provides critical compliance support to the clinical trial process by ensuring all study documentation is captured accurately in eCRFs.
  • Candidates must adhere to ICH, GCP, and other regulatory guidelines while managing multiple studies across various sites and regions.
  • The position involves acting as the primary point of contact for sponsors and supporting audit preparation to ensure readiness.

Matching Summary

Match Score: 75

** Thermo Fisher Scientific UK is seeking a Data Compliance Specialist to ensure accurate documentation and compliance within clinical trials. The role involves managing data entry in electronic case report forms (eCRF), conducting quality checks, and acting as a liaison between sponsors and site representatives. **

Skills & Requirements

Must-have

  • Clinical trial experience essential
  • eCRF data entry and accuracy
  • ICH GCP regulatory knowledge
  • Investigator Site File maintenance
  • Query resolution and tracking

Nice-to-have

  • Strong communication skills
  • Ability to work under pressure
  • Document management expertise
  • Time management capabilities
  • Problem solving methods

Key Requirements

  • Bachelor's degree or equivalent
  • 2+ years relevant clinical experience
  • Formal academic or vocational qualification

Work Rights

Not specified

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