Clinical Data Associate Iii

Thermo Fisher Scientific UK

Mexico City, Mexico
Whodd and meddra dictionaries
Edc systems (zelta, medidata rave, veeva)
Good clinical practice (gcp)
As part of the Clinical Data Management (CDM) team, the Coder of Clinical Data Management is responsible for coding medical terminology and reviewing coding listings in accordance with the Coding Plan and/or other related documentation

Job Summary

  • As part of the Clinical Data Management (CDM) team, the Coder of Clinical Data Management is responsible for coding medical terminology and reviewing coding listings in accordance with the Coding Plan and/or other related documentation.
  • The Coder must be able to efficiently organize the workload and code medical terminology in accordance with Good Clinical Practice (GCP), Standard Operating Procedures (SOPs)/Work Instructions (WIs) and other related documentation.
  • Thermo Fisher Scientific offers accessibility service for job seekers requiring accommodations in the job application process.

Matching Summary

As part of the Clinical Data Management (CDM) team, the Coder of Clinical Data Management is responsible for coding medical terminology and reviewing coding listings in accordance with the Coding Plan and/or other related documentation.

Skills & Requirements

Must-have

  • WHODD and MedDRA dictionaries
  • EDC systems (Zelta, Medidata Rave, Veeva)
  • Good Clinical Practice (GCP)
  • Standard Operating Procedures (SOPs)/Work Instructions (WIs)
  • clinical/medical terminology
  • regulatory guidelines

Nice-to-have

  • customer focus
  • interpersonal skills
  • flexibility and adaptability
  • team environment
  • independent work

Key Requirements

  • 4 or more years' experience
  • Bachelor’s degree or equivalent
  • relevant coding certifications / experience
  • Strong English communication and writing skills

Work Rights

Not specified

Tailored Resume

Cover Letter