Senior Technical Consultant
Hälso- och sjukvård samt biovetenskap · Bioteknik och läkemedel · Klinisk forskning · Läkemedelsutveckling
I korthet
We are seeking a Senior Technical Consultant with 6-8 years of experience in Pharmacovigilance and 2-3 years in Veeva Vault Safety. The role involves supporting PV operations, configuring and maintaining Veeva systems, and ensuring regulatory compliance. A Bachelor's/Master's degree in a related field and Veeva Platform Certification are required.
Ansvarsområden
- Support end-to-end Pharmacovigilance activities (case processing, QC, reporting).
- Configure and maintain Veeva Vault Safety (workflows, objects, fields, permissions, reports).
- Participate in system upgrades, validation, UAT, and documentation.
- Liaise with business teams to translate requirements into functional/technical solutions.
- Provide user support, training, and troubleshooting.
- Ensure compliance with GxP, SDLC, CSV, and global PV regulations.
Krav
- 6–8 years of experience in Pharmacovigilance / Drug Safety.
- 2–3 years hands‑on experience in Veeva Vault Safety.
- Veeva Platform Certification (mandatory).
- Strong understanding of ICH, GVP, and global safety regulations.
- Experience with PV workflows, E2B(R3), and safety system configurations.
Önskade kvalifikationer
- Experience with safety integrations, migrations, or other PV systems (Argus/ARISg).
- Consulting or life sciences solution delivery background.
#Techno-Functional Consultant#Pharmacovigilance#Veeva Vault Safety#PV operations#GxP#SDLC#CSV#global PV regulations