Offer summary
Qualifications:
Life science or biomedical degree, Experience in pharmacovigilance submissions, eCTD sequencing experience preferred, Advanced English skills, C1 level, Strong multitasking and organization skills.Key responsabilities:
- Support client in safety reporting
- Perform submissions of aggregate reports
- Oversight of reports to Regulatory Authorities
- Quality control of safety reporting activities
- Participate in audits and develop quality documents