Medical Reviewer – VAF 432

Groupe ProductLife; Deutschland; Vor Ort; EUR 60.000 - 80.000; Vollzeit

Zusammenfassung

A life sciences company in Germany is seeking a French-speaking Medical Reviewer with a specialization in Dermatology. The role requires at least 5 years of experience in pharmacovigilance, proficiency in both French and English, and a strong understanding of GVP and FDA regulations. Key responsibilities include supporting assessments, mentoring, and ensuring client needs are met. This is an excellent opportunity to join a recognized organization dedicated to public health and regulatory excellence.

Qualifikationen

• Minimum 5 years experience in Pharmacovigilance with service providers or pharmaceutical companies.
• Experience with SUE assessments and Cosmetics Regulation Act.
• Deep understanding of pharmacovigilance principles and adverse event reporting.

Aufgaben

• Support in seriousness assessment including Initial Triage.
• Mentor junior medical reviewers.
• Participate in audits and inspections.

Kenntnisse

French speaking

English proficiency

Client communications

Understanding of GVP and FDA regulations

Organizational skills

Emotional intelligence

Analytical thinking

Ausbildung

MBBS or MD specializing in Dermatology

Tools

Microsoft Office

Safety databases

Jobbeschreibung

ProductLife Group is looking for an experienced,French speakingMedical 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

• 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:
• 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, andcosmetic 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.