Global Pharmacovigilance Project Lead

Ergomed; Madrid; Presencial; EUR 60.000 - 90.000; Jornada completa

Descripción de la vacante

Ergomed Group in Madrid, Spain, is seeking a PV Project Manager to lead client-facing pharmacovigilance projects, ensuring safety data quality and timely delivery.

You will coordinate cross-functional teams, develop project scopes from signed agreements, plan activities and milestones, and report progress to clients and internal stakeholders.

The role requires a health or life science background and the ability to communicate at senior levels within pharmaceutical organizations.

Formación

• Proven track record of demonstrated Pharmacovigilance activities including processing and quality review of ICs, literature screening, reconciliation, and preparation of SOPs.
• PV Project Management experience from ideally a service provider / CRO.
• Be comfortable with communicating at senior levels within pharmaceutical organizations.

Responsabilidades

• Acting as the primary contact point for project-related matters
• Managing client’s expectations to make sure the client is satisfied with services of PrimeVigilance, and that the work PrimeVigilance delivers meets, or even exceeds, the clients’ expectations.
• Preparing project scope and objectives based on the signed agreement between the client and PrimeVigilance.
• Project activities planning, including deadlines and interim milestones
• Reporting for the client and the PrimeVigilance management, e.g., preparation of Monthly reports, serving as basis for invoicing.

Conocimientos

Pharmacovigilance experience

PV project management

Senior stakeholder communication

Leadership and mentoring

Educación

Health Care Professional or Life Science Graduate

Descripción del empleo

Ergomed Group in Madrid, Spain, is seeking a PV Project Manager to lead client-facing pharmacovigilance projects, ensuring safety data quality and timely delivery.

You will coordinate cross-functional teams, develop project scopes from signed agreements, plan activities and milestones, and report progress to clients and internal stakeholders.

The role requires a health or life science background and the ability to communicate at senior levels within pharmaceutical organizations.