Pharmacovigilance Program Director

ProductLife Group; Lyon; Sur place; EUR 60 000 - 100 000; Plein temps

Résumé du poste

An innovative firm is seeking a dedicated Program Director in Pharmacovigilance to lead client projects and ensure compliance with regulatory standards. This role involves managing client relationships, monitoring key performance indicators, and supporting quality control efforts. The ideal candidate will possess a strong pharmaceutical background and deep knowledge of pharmacovigilance principles, with the ability to communicate effectively in both English and French. Join this dynamic team to make a significant impact in the field of drug safety and client relations.

Qualifications

• Minimum 5-10 years experience in service providers.
• Strong understanding of GVP, GCP, FDA regulations.

Responsabilités

• Manage client relationships and act as the main point of contact.
• Monitor client KPIs and ensure regulatory compliance.

Connaissances

Effective communication skills

Fluency in English

Fluency in French

Analytical skills

Flexibility

Reliability

Punctuality

Formation

Pharmaceutical background

5-10 years experience in service providers

Description du poste

ProductLife Group is looking for a dedicated Program Director (Pharmacovigilance) to join our dynamic team to oversee and contribute to the activities performed in the Hub :

Responsibilities :

• Manage relationships with larger client projects and act as single point of contact for the client
• Monitor client KPI
• Support in the resolution of NC / CAPA, identify RCA and implement improvements
• Perform Quality Control / Medical Review and provide support to the team where necessary to ensure regulatory compliance
• Participate in audits and inspections as required
• Ensure understanding of client needs and ensure expectations are met and exceeded
• Organise team meetings as requested

Education and Experience :

• Minimum 5-10 years experience working for service providers
• Pharmaceutical background – strong understanding of GVP, GCP, FDA and regulatory requirements related to drug safety.
• Deep knowledge of pharmacovigilance principles, adverse event reporting, causality assessment
• Previous experience working to deadlines.
• Client communications

Skills :

• Effective communications skills both written and verbal to be able to explain complex concepts and address queries from the team.
• Fluent in both English and French
• Ability to deliver constructive feedback
• Analytical skills
• Flexibility
• Reliable
• Punctual