Clinical Data Specialist Iii

Thermo Fisher Scientific UK

Not specified (likely office-based, as indicated by "environmental conditions office").
Knowledge of ich and gcp guidelines
Experience in pharmaceutical or biotech industry
Understanding of clinical trial process phases i-iv
Thermo Fisher Scientific is seeking a Clinical Data Specialist III to join their team, focusing on clinical data management and project coordination in the biotechnology or pharmaceutical sector. The ideal candidate will possess strong communication and organizational skills, with a comprehensive understanding of clinical trial processes and regulations

Job Summary

  • The role involves collaborating with stakeholders to develop effective clinical data project plans including scope, goals, and deliverables.
  • Candidates must ensure their team executes Clinical Data Management functions in accordance with CorEvitas Standard Operating Procedures.
  • Thermo Fisher Scientific offers a mission-driven environment where diverse experiences are valued to accelerate research and solve complex scientific challenges.

Matching Summary

Match Score: 85

Thermo Fisher Scientific is seeking a Clinical Data Specialist III to join their team, focusing on clinical data management and project coordination in the biotechnology or pharmaceutical sector. The ideal candidate will possess strong communication and organizational skills, with a comprehensive understanding of clinical trial processes and regulations.

Skills & Requirements

Must-have

  • Knowledge of ICH and GCP guidelines
  • Experience in pharmaceutical or biotech industry
  • Understanding of clinical trial process phases I-IV
  • Strong project management and organizational skills
  • Ability to resolve data queries and risks

Nice-to-have

  • Phase IV and Real-World Evidence experience
  • Team-oriented mindset with initiative
  • Professional demeanor under high stress
  • Experience with observational registries

Key Requirements

  • Bachelor's degree required
  • Minimum 2 years pharmaceutical/biotech experience
  • Minimum 3 years data experience
  • Comprehensive knowledge of CFR, GCP, and ICH Guidelines

Work Rights

Not specified

Tailored Resume

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