- Mexico City, Mexico City, Mexico
- Associate
- 1–2 years
Review, assess and process Safety data and information, across service lines, received from various sources and distribute reports/data onwards to both internal and external third parties following applicable regulations SOPs and internal guidelines under guidance and support of senior operation team members.
Responsibilities
- Process Safety data according to applicable regulations, guidelines, Standard Operating procedures (SOPs) and project requirements
- Perform Pharmacovigilance activities including collecting and tracking incoming Adverse Events(AE)/endpoint information
- Database entry
- Coding AE and Products, writing narratives, Literature related activities
- Ensure to meet quality standards per project requirements
Requirements
- Bachelor’s degree in Life sciences or a related field
- Nice to have: Pharmacovigilance experience
- Nice to have: Experience with Safety Databases (ARGUS or others)
- Nice to have: Knowledge of applicable global, regional, local clinical research regulatory requirements
- Nice to have: Excellent attention to detail and accuracy