As a Regulatory Affairs Consultant you will be joining the world’s largest & most comprehensive clinical research organisation, powered by healthcare intelligence.
**What you will be doing**:
- Excellent understanding of Cofepris regulations for drug promotion/advertising and labeling, and experience interacting with Cofepris
Experience with Veeva Vault PromoMats or similar document management systems a plus
Demonstrated expertise in regulatory requirements for labeling and advertising materials.
- Experience in reading, interpreting, and evaluating regulatory guidance documents and initiating changes in systems to ensure regulatory compliance.
- Knowledge of Common Technical Document and global guidelines on content and format of labeling preferred.
- Experience with creating and reviewing labeling and advertising materials required.
- Experience on collaborative multifunctional work teams at the local or global level.
- Ability to manage multiple tasks and ...