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Consultant – Safety Periodic Reports Lead
Ividata Life SciencesConsultant - Safety Periodic Reports Lead at IVIDATA Life Sciences. Collaborating on projects in pharmacovigilance with a dynamic team.
About the role
Key responsibilities & impact- Participates in the planning, coordination and production of periodic safety deliverables
- Contributes to the ongoing assessment of products' benefit–risk profiles and to the identification of safety issues
- Supports the preparation, update and monitoring of risk management plans and measures
- Coordinates internal and external contributions required for the production of safety documents
- Ensures compliance with regulatory requirements, deadlines and quality standards
- Takes part in project meetings and cross-functional discussions as the safety point of contact
Requirements
What you’ll need- Doctorate in medicine, pharmacy or life sciences
- Additional training or certification in pharmacovigilance/drug safety highly desirable
- Proven experience in pharmacovigilance/drug safety, ideally with products of international scope
- Rigour and a strong sense of responsibility, with a solid quality and compliance mindset
- Professional-level English fluency required (written and spoken)
Benefits
Comp & perks- Remote work possible
- Stimulating, collaborative work environment
ATS Keywords
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Hard Skills & Tools
pharmacovigilancerisk managementsafety assessmentbenefit-risk profile analysissafety document production
Soft Skills
rigourresponsibilityquality mindsetcompliance mindsetcommunication
Certifications
Doctorate in medicineDoctorate in pharmacyDoctorate in life sciencesCertification in pharmacovigilance