Remote Pharmacovigilance Project Lead

PrimeVigilance; Lisboa; Presencial; EUR 35 000 - 52 000; Tempo integral

Resumo da oferta

PrimeVigilance in Lisbon, Portugal, is seeking a pharmacovigilance professional to support project activities for clients and the company. You will create and maintain project KPIs for contracted ICSR work, optimize procedures and trainings, and propose changes to the ICSR Lead.

You will also manage deviations and ensure data accuracy across trackers and timesheets. You will operate as the team SME for ICSR, provide cross‑department support, and may act as LCPPV for the country and PRLS for the

Qualificações

• Life science graduate or related healthcare qualification.
• 3–4 years of pharmacovigilance experience with at least 1 year in line management.
• Excellent written and verbal communication skills.
• Strong organization, multitasking and time management abilities.
• Ability to delegate effectively and work in a team.
• Fluent English (written and spoken).

Responsabilidades

• Provide support to project team activities for the client and company.
• Create and maintain project KPIs for contracted ICSR activities; optimize procedures and trainings.
• Propose process changes to the ICSR Operational Lead.
• Manage ICSR deviations with ICSR Operational Lead support.
• Review trackers and timesheet data for accuracy.
• Perform ICSR processing and 2nd QC of cases.
• Support other departments as needed.
• Serve as the SME for the ICSR team; support RA & PV Network; act as LCPPV for the specified country and PRLS for the designated language, as agreed.

Conhecimentos

Excellent communication

Organization skills

Delegation skills

Planning and time management

Team working

English fluent

Formação académica

Life science degree

Descrição da oferta de emprego

PrimeVigilance in Lisbon, Portugal, is seeking a pharmacovigilance professional to support project activities for clients and the company. You will create and maintain project KPIs for contracted ICSR work, optimize procedures and trainings, and propose changes to the ICSR Lead.

You will also manage deviations and ensure data accuracy across trackers and timesheets. You will operate as the team SME for ICSR, provide cross‑department support, and may act as LCPPV for the country and PRLS for the