Global Patient Safety Asset Lead, Rare Diseases

Ipsen; England; On-site; GBP 120,000 - 155,000; Full time

Job summary

Ipsen is seeking a Global Patient Safety Asset Lead, Rare Diseases, based in London. The role represents GPS in Global Asset and Clinical Development Teams, ensuring proactive safety surveillance and risk management for assigned products throughout development and lifecycle.

Ideal candidates have an MD with clinical development leadership experience, strong pharmacovigilance knowledge, and fluency in English.

Qualifications

• MD with clinical experience exercising medical judgment as a physician.
• Experience leading Clinical Development Teams is ideal.
• Pharmaceutical industry experience in clinical development and cross-functional teamwork.

Responsibilities

• Represent GPS as a member of Global Asset Team and Clinical Development Team for products.
• Accountable for safety surveillance and risk management to ensure safe use in development and on market.
• Lead safety governance and provide strategies to regulatory submissions and PSURs/DSURs.
• Provide leadership to global filing teams for regulatory submissions and authority interactions.
• Contribute to cross-functional teams and external meetings where safety matters are discussed.

Skills

Pharmacovigilance leadership

Cross-functional leadership

Safety surveillance

Medical judgment

Education

MD

Tools

Regulatory submissions (NDA/BLA)

Job description

Company: Ipsen Pharma (SAS)
Location: Paris, London (UK)
Time Type: Full time
Job Requisition ID: R-22023
About Ipsen
Ipsen is a mid-sized global biopharmaceutical company with a focus on transformative medicines in three therapeutic areas: Oncology, Rare Disease and Neuroscience. Supported by nearly 100 years of development experience, with global hubs in the U.S., France and the U.K, we tackle areas of high unmet medical need through research and innovation.
Our passionate teams in more than 40 countries are focused on what matters and endeavor every day to bring medicines to patients in 88 countries. We build a workplace that champions human-centric leadership and fosters a culture of collaboration, excellence and impact. At Ipsen, every individual is empowered to be their true selves, grow and thrive alongside the company’s success. Join us on our journey towards sustainable growth, creating real impact on patients and society!
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Are you ready to lead and innovate in a dynamic, patient-focused biopharmaceutical company?
Ipsen is a growing global specialty-driven biopharmaceutical company focused on innovation and specialty care. We aim to make a sustainable difference by significantly improving patients’ health and quality of life, providing effective therapeutic solutions for unmet medical needs through differentiated and innovative medicines in Oncology, Neurosciences, and Rare Diseases.
Why Ipsen?

• Patient-Focused: The patient is at the heart of everything we do, and improving their outcomes is the deliverable of every strategy.
• Employee Care: We care for our employees, who are the ambassadors making a real difference.
• Bold Leadership: We attract and develop bold, agile, entrepreneurial individuals who take full ownership of their decisions.
• Growth Opportunities: We offer a wealth of fulfilling challenges and growth opportunities in a fast-moving, game-changing organization.

About the Role
The Global Patient Safety Asset Lead, Rare Diseases is:

• Representing Global Patient Safety (GPS) as a member of the Global Asset Team and Clinical Development Team for one or more products, as required and as delegated by the respective GPS TA Leader, and as such be the contact person for relevant safety-related deliverables, issues and questions in relation to this (these) product(s).
• Accountable for the conduct of safety surveillance and assessment of integrated safety information, to ensure the timely proposal of changes to the safety profile and appropriate risk management and risk minimization actions, in order to warrant the safe and effective use of Ipsen product in development projects and on the market.

This requires effective medical, technical and scientific expertise in safety data collection, evaluation, medical interpretation and communication. Ideally, requires also experience in leading Safety Teams and Cross functional Global Asset Teams and Clinical Development Teams.

Main Responsibilities
Ensure proactive safety and risk management for all assigned products

• Implement proactive safety and risk management strategies, agreed cross-functionally with asset team colleagues for assigned products, integrated with clinical development and life-cycle management plans for milestone decisions
• Ensure that clinical development plans/life-cycle management plans adequately address the safety questions and deliver the safety strategy for approval by safety governance
• Ensure that all safety-based decisions for benefit-risk assessment are taken in the knowledge of a comprehensive assessment of all available evidence
• Provide safety expertise, strategies and leadership to the global filing teams for all components of regulatory submissions, health authority questions, and periodic safety reports (PSURs, PBRERs, DSURs)
• Contribute effectively to internal interactions and cross-functional teams

Ensure up-to-date oversight of the emerging safety profile for all TA products

• Ensure continuous assessment of all new safety information, in collaboration with the Safety Team and Cross functional Teams
• Lead signal detection and signal evaluation activities for assigned products

Provide strong safety representation at internal and external meetings where safety issues are considered, and/or safety decisions are made

• Contribute effectively in external interactions, e.g., SMCs/IDMCs; preparation of the medical safety aspects for, and attendance at, regulatory authority meetings; interactions with external advisers or opinion leaders; collaboration with colleagues from partnership companies for co-development or co-marketing etc.

Contribute to the overall success of Global Patient Safety and Ipsen

• Provide TA and product-specific training within GPS and more widely within the company and for external vendors as required

Qualifications

• MD, with several years of clinical experience exercising medical judgment as a physician
• Experience in leading Clinical Development Teams is ideal
• Pharmaceutical industry experience in clinical development
• Experience in leading Cross functional Global Product Teams, Safety Teams and Clinical Development Teams.
• Knowledge of product development processes and experience of cross-functional teamwork
• Working knowledge of pharmacovigilance legislations worldwide
• Prior experience with NDA/BLA or equivalent regulatory submissions, or experience working in a Regulatory Agency reviewing submission file
• Fluent in English, additional European language such as French is preferrable

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Nous nous engageons à créer un lieu de travail où chacun se sent écouté, valorisé et soutenu, où nous incarnons « The Real Us*. La valeur que nous accordons aux différentes perspectives et expériences motive notre engagement en faveur de l'inclusion et de l'égalité des chances. Lorsque nous intégrons des modes de pensée diversifiés, nous prenons des décisions plus réfléchies et découvrons des solutions plus innovantes. Ensemble, nous nous efforçons de mieux comprendre les communautés que nous servons. Cela signifie que nous voulons également vous aider à donner le meilleur de vous-même lorsque vous postulez à un poste chez nous. Si vous avez besoin d'aménagements ou d'aide pendant le processus de candidature, veuillez en informer l'équipe de recrutement. Ces informations seront traitées avec soin et n'auront aucune incidence sur le résultat de votre candidature. *Soyons nous-même

Global Patient Safety Asset Lead, Rare Diseases London, United Kingdom