Fsp - Regulatory And Start Up Specialist

IQVIA UK

Sao Paulo, SP, Brazil
Hybrid
Cep/conep submission experience
Icf country customization skills
Anvisa regulatory knowledge
The role serves as a Single Point of Contact for feasibility, site activation, and maintenance activities in assigned studies

Job Summary

  • The role serves as a Single Point of Contact for feasibility, site activation, and maintenance activities in assigned studies.
  • Candidates must possess advanced knowledge of Brazilian regulatory requirements including CEP/CONEP, ANVISA submissions, and ICF adaptations.
  • This hybrid position is based in Sao Paulo, SP, offering the opportunity to work with a leading global provider of clinical research services.

Matching Summary

The role serves as a Single Point of Contact for feasibility, site activation, and maintenance activities in assigned studies.

Skills & Requirements

Must-have

  • CEP/CONEP submission experience
  • ICF country customization skills
  • ANVISA regulatory knowledge
  • Site activation and maintenance
  • Contract negotiation with sites

Nice-to-have

  • Strong communication skills
  • Team collaboration abilities
  • Advanced English proficiency

Key Requirements

  • Bachelor's Degree in Life Sciences
  • 1-2 years CRO or Pharma regulatory experience
  • Experience with CEP/CONEP and ANVISA processes

Work Rights

Not specified

Tailored Resume

Cover Letter