Global Head of Pharmacovigilance

BioTalent; Essen; Hybrid; EUR 120.000 - 160.000; Vollzeit

Zusammenfassung

A leading biotech firm in Germany is seeking a Global Head of Pharmacovigilance. This strategic role focuses on drug safety and compliance, requiring 12–15+ years of experience, particularly in oncology. The successful candidate will lead pharmacovigilance strategy and manage high-performing teams. Proficiency in drug safety regulations and a medical degree are essential. This position offers flexible hybrid or remote work arrangements.

Qualifikationen

• 12–15+ years experience in drug safety or pharmacovigilance.
• 5+ years in a senior leadership role in biotech or pharma.
• Oncology experience required.

Aufgaben

• Develop and execute drug safety and pharmacovigilance strategy.
• Oversee safety surveillance and risk assessment.
• Ensure compliance with international PV regulations.

Kenntnisse

Drug safety management

Regulatory compliance

Team leadership

Pharmacovigilance strategy

Communication skills

Ausbildung

Medical degree (MD, MBBS, DO)

Tools

Safety databases (e.g., Argus)

Coding dictionaries (MedDRA)

Jobbeschreibung

Overview

BioTalent are delighted to partner with a rapidly growing biotech client, dedicated to transforming cancer treatment, currently hiring for a Global Head of Pharmacovigilance.

This is a strategic leadership role responsible for guiding safety strategy, ensuring compliance, and driving successful trial conduct for company assets across all stages of development. This role directs safety strategy, operations, and regulatory compliance for oncology drug products across clinical development and commercialization phases, and is central to ensuring safe, compliant, and successful oncology drug development and to maximizing patient safety from clinical trials to post-marketing surveillance.

This position will report to the Chief Medical Officer and can be based on a hybrid basis from the company office in Germany or on a remote basis.

Your mission

• Develop and execute the overall drug safety and pharmacovigilance (PV) strategy aligned with company and global regulatory requirements, especially for oncology assets.
• Oversee safety surveillance, signal detection, risk assessment, and risk mitigation for investigational and marketed oncology products.
• Ensure compliance with international PV regulations (FDA, EMA, ICH), SOPs, and best industry practices.
• Lead and build high-performing PV teams, including medical safety experts and regulatory specialists, fostering a collaborative and high-performance culture.
• Medical oversight of safety data, including the review of case safety reports (SAEs, SUSARs) and aggregate analyses.
• Establish and maintain risk management plans, safety monitoring plans, data exchange agreements, and readiness for health authority inspections.
• Represent the company in safety-related interactions with regulatory agencies, partners, and external stakeholders.
• Collaborate cross-functionally with clinical development, regulatory, medical affairs, and other teams integrating safety across the product lifecycle.

Ideal candidate

• A medical degree (MD, MBBS, DO) or equivalent clinical degree.
• 12–15+ years experience in drug safety / pharmacovigilance with at least 5 years at a senior leadership level in biotech and pharma.
• Oncology experience is required.
• Experience with Antibody Drug Conjugates (ADCs) is a strong plus.
• In-depth knowledge of global PV regulations and experience with safety and efficacy submissions (IND, BLA, NDA, MAA).
• Experience with risk management plans, signal detection, aggregate safety data review, and case management.
• History of building, leading, and mentoring multidisciplinary teams.
• Familiarity with major safety databases (e.g., Argus), coding dictionaries (MedDRA), and digital safety systems.
• Outstanding communication skills and proven ability to influence, collaborate, and present safety strategy to senior leaders and regulatory authorities.
• Strategic decision-making abilities and the capacity to oversee budgets, resources, and department objectives in a dynamic environment.
• Fluency in English.

How to apply

If interested, please apply using the link or reach out to Ella Jobson on [phone]