Medical Reviewer – VAF 432

ProductLife Group; Courbevoie; Sur place; EUR 60 000 - 80 000; Plein temps

Résumé du poste

A global life sciences company is looking for an experienced Medical Reviewer to contribute to pharmacovigilance efforts. This role requires a medical degree and at least 5 years of relevant experience. Bilingual in French and English is essential, with further languages as a plus. Key responsibilities include supporting seriousness assessments, mentoring junior staff, and participating in audits. The company promotes a collaborative culture and offers professional growth within a dynamic organization dedicated to public health.

Prestations

Flexible work arrangements

Professional development opportunities

Collaborative work environment

Supportive culture

Qualifications

• 5+ years experience in a Pharmacovigilance department at a service provider or pharmaceutical company.
• Proficiency in English and French languages; additional languages are a plus.
• Strong understanding of GVP, FDA regulations, and cosmetic regulations.

Responsabilités

• Support in seriousness assessment, Initial Triage, and causality evaluations.
• Mentor junior medical reviewers and perform additional review of cases.
• Participate in audits and ensure client's needs are met.

Connaissances

Pharmacovigilance

Client communications

Regulatory expertise

Effective written and verbal communication

Emotional intelligence

Formation

MBBS or MD (Doctor of Medicine) specializing in Dermatology

Outils

Microsoft Office

Safety databases

Description du poste

ProductLife Group is looking for an experienced, French speaking Medical Reviewer.

Why Join ProductLife Group?

At ProductLife Group (PLG), we’re a trusted global partner in life sciences, dedicated to improving public health through regulatory excellence and innovation. As a Medical Reviewer, you’ll be part of a growing international team with the opportunity to :

🌍 Collaborate Globally : Work with international teams on diverse regulatory and clinical projects.

🧠 Grow Your Expertise : Deepen your knowledge in pharmacovigilance, clinical trials, and therapeutic areas with professional development opportunities. This role can be a stepping stone to significant career progression in PLG’s rapidly growing pharmacovigilance business unit.

🚀 Develop Within a Dynamic Platform : Be part of a fast-evolving organization that values continuous learning.

🤝 Thrive in a Balanced & Supportive Culture : Enjoy flexible work arrangements and a collaborative environment that supports your well-being.

🏆 Work for a Recognized Leader : Certified as a Great Place to Work, PLG fosters trust, growth, and inclusion.

🌐 Make a Real Impact : Play a key role in advancing public health through meaningful medical review contributions.

Key Responsibilities

Post‑Marketing (Pharmacovigilance)

• Support in seriousness assessment including Initial Triage
• Support in causality, medical assessment, MedDRA coding.
• Mentor junior medical reviewers and perform additional review of cases to ensure competency.
• Participate in audits and inspections as required
• Ensure understanding of client needs, conventions and ensure expectations are met and exceeded
• Training and mentoring other team members

Qualifications & Skills

• Education: MBBS or MD (Doctor of Medicine) – Specializing in Dermatology
• Experience of SUE assessments
• Cosmetics Regulation Act
• Client communications
• Safety Database experience
• Minimum 5 years experience working for service providers or pharmaceutical company in Pharmacovigilance department

Languages: French AND English (Native / Fully professional); any additional languages are a plus

Technical Skills

• Proficiency in Microsoft Office
• Strong understanding of GVP, FDA regulations, and cosmetic regulations and regulatory requirements related to drug / cosmetic safety.
• Deep knowledge of pharmacovigilance principles, adverse event reporting, causality assessment
• Solid medical knowledge and Pharmacology understanding
• MSSO- MedDRA

Additional Skills

• Effective written and verbal communication
• Clinical experience (preferred)
• Emotional intelligence, adaptability, and analytical thinking
• Strong organizational skills, reliability, and punctuality
• Experience with safety databases

Join ProductLife Group and be part of a mission-driven team that’s shaping the future of drug safety and public health.