At a Glance
- Tasks: Lead safety strategies for innovative medicines in rare diseases and ensure patient safety.
- Company: Ipsen Pharma, a global biopharmaceutical leader focused on transformative medicines.
- Benefits: Competitive salary, employee care, growth opportunities, and a collaborative culture.
- Other info: Join a diverse team committed to inclusion and innovation.
- Why this job: Make a real impact on patients' lives while working with cutting-edge therapies.
- Qualifications: MD with clinical experience and leadership in clinical development teams.
The predicted salary is between 54574 - 66702 £ per year.
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 endeavour 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.
Job Description: 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 responsible for representing Global Patient Safety (GPS) as a member of the Global Asset Team and Clinical Development Team for one or more products. This role includes being the contact person for relevant safety-related deliverables, issues and questions in relation to these products. The individual will be accountable for the conduct of safety surveillance and assessment of integrated safety information, ensuring timely proposals of changes to the safety profile and appropriate risk management actions.
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.
- Ensure that clinical development plans adequately address safety questions and deliver the safety strategy for approval by safety governance.
- Support safety decision making for benefit-risk assessment.
- Provide safety expertise, strategies and leadership to the global filing teams for regulatory submissions and periodic safety reports.
- Contribute effectively to internal interactions 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.
- 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.
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.
- Knowledge of product development processes and experience of cross-functional teamwork.
- Working knowledge of pharmacovigilance legislations worldwide.
- Fluent in English, additional European language such as French is preferable.
Location: Paris; London (UK)
Type: Full time
Global Patient Safety Asset Lead, Rare Diseases in London employer: Ipsen
Ipsen in Wrexham is an excellent employer, offering a collaborative work culture that prioritises innovation and excellence. Employees benefit from a supportive environment with opportunities for professional growth, all while working in a state-of-the-art packing facility that operates on a convenient Monday to Friday schedule. Join us to be part of a team that values your expertise and contributions in mechanical engineering and vision systems.
StudySmarter Expert Advice🤫
We think this is how you could land Global Patient Safety Asset Lead, Rare Diseases in London
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Get involved with organisations such as the Royal Pharmaceutical Society or your local pharmaceutical professionals' network. Being an active member can boost your credibility and may even lead to job referrals in top organisations like Ipsen.
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We think you need these skills to ace Global Patient Safety Asset Lead, Rare Diseases in London
Some tips for your application 🫡
Showcase Your Relevant Experience:When applying for a role in the pharmaceutical industry, it's crucial to highlight any relevant experience you have. Whether that's internships, lab work, or even related coursework, make sure to weave this into your CV and cover letter. We want to see how your background aligns with the role you're applying for at Ipsen!
Emphasise Your Understanding of Regulations:The pharmaceutical industry is heavily regulated, so it's important to indicate your familiarity with industry standards and regulations. In your cover letter, mention any training or certifications you've received that are relevant, or discuss projects where you’ve navigated compliance. This will show Ipsen that you're not just a fit for the job but also a safety-conscious candidate!
Tailor Your CV to Be Result-Driven:Craft your CV to highlight quantifiable achievements, especially if you have previous roles in pharmaceuticals or related fields. Use metrics to demonstrate your impact, such as improved processing times or successful project completions while working on trials. This analytical approach will resonate well with hiring managers at Ipsen!
Convey Your Passion for the Industry:In your cover letter, express why you are passionate about working in the pharmaceutical sector. Whether it’s your desire to contribute to groundbreaking drug research or improve patient outcomes, let it shine through! At Ipsen, we value candidates who are truly enthusiastic about their work—you might just stand out from the crowd.
How to prepare for a job interview at Ipsen
✨Understand the Science
Make sure you brush up on key pharmaceutical concepts and recent developments in the industry. You might get asked some technical questions during the interview at Ipsen that show your grasp of drug development processes or regulatory requirements, so be ready to discuss them clearly.
✨Showcase Relevant Experience
If you have any hands-on experience or internships in a laboratory setting, be sure to highlight these in your responses. Think about the projects you worked on, the methodologies you used, and the impact you made. It's all about telling a story that connects your background to the role you're applying for.
✨Know Their Products
Take some time to familiarise yourself with Ipsen’s product range and recent breakthroughs. Understanding their portfolio not only shows your enthusiasm for the role but also allows you to ask insightful questions that demonstrate your interest in actively contributing to their projects.
✨Be Ready for Regulatory Scenarios
In a full-time pharmaceutical role, understanding the regulatory landscape is crucial. Prepare for situational questions that may test your problem-solving skills concerning compliance and safety standards. You could be asked how you'd handle a hypothetical issue regarding a drug’s market release, so think through your approach.
