Associate / Sr. Associate - Medicines Quality Organization (Pharmacovigilance)
Eli Lilly
- Cork
- Permanent
- Full-time
- Bachelor’s Degree in a science/health care related field or equivalent work experience
- Demonstrated ability to apply quality systems within a regulated work environment
- Strong understanding of pharmacovigilance regulations and guidelines.
- Effective project and time management skills
- Knowledge of GCP, ICH, FDA, and other regulatory requirements
- Demonstrated ability to communicate effectively, both written and verbal, and to influence others
- Demonstrated ability to prioritize and handle multiple concurrent tasks
- Cognitive abilities which include problem solving, verbal reasoning, attention to detail, critical thinking and analytical competencies
- Strong interpersonal skills with demonstrated flexibility in varying environments/geographies
- Effective organization/self-management skills
- Minimum of three years’ experience in clinical trials and/or pharmacovigilance
- Proficiency in pharmacovigilance software and databases.
- Experience in a quality control/quality assurance role
- Experience in defined functional business areas, for example, safety management
- Knowledge of quality systems
- Ability to work independently and as part of a team
- Demonstrated ability to work in a global environment