At a Glance
- Tasks: Manage drug safety operations and ensure compliance with pharmacovigilance regulations.
- Company: Leading pharmaceutical company dedicated to improving patient lives.
- Benefits: Competitive salary, health benefits, and opportunities for professional growth.
- Other info: Dynamic team environment with a focus on collaboration and impact.
- Why this job: Make a real difference in patient safety and contribute to innovative medicines.
- Qualifications: Scientific degree and experience in pharmacovigilance preferred.
The predicted salary is between 40000 - 50000 € per year.
If you’re passionate about changing lives for the better, this is the opportunity you’ve been waiting for. In Research & Development - Drug Safety, we’re continuously exploring innovative new treatment options to make a stronger, more positive impact on the lives of the patients we serve. You’ll work with talented colleagues in a state-of-the-art Research & Development environment, developing innovative medicines that change the life of patients for the better and help us make progress towards our vision of a world free of pain. Join us today, and discover the difference you can make.
What the job looks like
- Drug Safety operations for the local pharmacovigilance system and Deputy Local Responsible Person for Pharmacovigilance (LRP-PV) for United Kingdom, Ireland and Nordics (UKINOR) with the Local Drug Safety department.
- Work with and deputize for the LRP-PV to maintain a local pharmacovigilance system to perform tasks to comply with national pharmacovigilance requirements and company standards to ensure products maintain favorable benefit safety profile.
- Assist the LRP-PV in supporting the local commercial business, Drug Safety business continuity, and back up processes.
- Active in maintaining the local pharmacovigilance system including tasks such as procedural updates, training personnel, deviation and CAPA management, audit/inspection support and monitoring for changes in local pharmacovigilance regulations.
- Assist in drug safety agreement and service provider management.
- Monitor, collect and follow-up of safety information (signals, spontaneous and solicited cases) from different sources/channels (e.g. digital/social media, organized data collection programmes, local literature); manage and report safety cases internally through existing systems and procedures.
- Assist in management of pharmacovigilance requests (e.g. questions, local data required for safety report generation), audits and inspections.
- Support the implementation and monitoring of safety measures locally for patient safety (e.g. implementation of additional risk minimization measures).
- Quality control checks, filing, tracking, and archiving of the local pharmacovigilance related documentation (e.g. safety cases, safety data outputs).
- Collaborate within Global Drug Safety in Drug Safety international tasks/projects across territories to support pharmacovigilance activities.
What you’ll bring to the table
- Language skills: Business English; Nordic language skills beneficial.
- Microsoft based and general IT competence.
- Proactive and solution orientated to contribute to a high performing pharmacovigilance system and being patient-centric.
- Ability to work within an international matrix Drug Safety environment.
- Passion for pharmacovigilance.
- Relevant experience/understanding of the pharmaceutical industry, with a strong focus on pharmacovigilance operations within a local affiliate.
- Scientific /(para)medical degree (e.g. pharmacist, biological sciences).
- Ability to attend the Maidenhead office as required.
Associate Drug Safety Manager (UK, Ireland, Nordics) in Maidenhead employer: Grünenthal Group
As an Associate Drug Safety Manager, you will be part of a dynamic team dedicated to improving patient lives through innovative drug safety practices. Our state-of-the-art Research & Development environment fosters a collaborative work culture that prioritises employee growth and development, offering numerous opportunities for professional advancement. Located in Maidenhead, we provide a supportive atmosphere where your contributions directly impact the safety and efficacy of our medicines, making this an exceptional place to build a meaningful career.
StudySmarter Expert Advice🤫
We think this is how you could land Associate Drug Safety Manager (UK, Ireland, Nordics) in Maidenhead
✨Tip Number 1
Network like a pro! Reach out to professionals in the drug safety field on LinkedIn or at industry events. A friendly chat can open doors that a CV just can't.
✨Tip Number 2
Prepare for interviews by researching the company and its recent projects. Show them you’re not just another candidate; you’re genuinely interested in their mission to change lives.
✨Tip Number 3
Practice your answers to common interview questions, especially those related to pharmacovigilance. We want you to feel confident and ready to showcase your passion and expertise!
✨Tip Number 4
Don’t forget to apply through our website! It’s the best way to ensure your application gets the attention it deserves. Plus, we love seeing candidates who are proactive about their job search.
We think you need these skills to ace Associate Drug Safety Manager (UK, Ireland, Nordics) in Maidenhead
Some tips for your application 🫡
Show Your Passion:When you're writing your application, let your passion for drug safety and making a difference shine through. We want to see how your enthusiasm aligns with our mission to change lives for the better!
Tailor Your CV:Make sure your CV is tailored to highlight your relevant experience in pharmacovigilance. We love seeing how your background fits with the role, so don’t be shy about showcasing your skills and achievements!
Be Clear and Concise:Keep your application clear and to the point. We appreciate straightforward communication, so avoid jargon and make it easy for us to see why you’re the perfect fit for the Associate Drug Safety Manager role.
Apply Through Our Website:Don’t forget to apply through our website! It’s the best way for us to receive your application and ensures you’re considered for this exciting opportunity. We can’t wait to hear from you!
How to prepare for a job interview at Grünenthal Group
✨Know Your Pharmacovigilance Basics
Make sure you brush up on your knowledge of pharmacovigilance systems and regulations. Understand the local requirements for the UK, Ireland, and Nordics, as well as any recent changes in legislation. This will show your passion for the field and your commitment to patient safety.
✨Showcase Your Problem-Solving Skills
Prepare examples from your past experiences where you've had to tackle challenges in drug safety or pharmacovigilance. Highlight how you approached these issues proactively and what solutions you implemented. This will demonstrate your solution-oriented mindset, which is crucial for this role.
✨Familiarise Yourself with the Company’s Vision
Research the company’s mission and values, especially their focus on innovative treatment options and patient-centric approaches. Be ready to discuss how your personal values align with theirs and how you can contribute to their vision of a world free of pain.
✨Practice Your Communication Skills
Since you'll be working in an international matrix environment, it's essential to communicate effectively. Practice articulating your thoughts clearly and concisely, especially when discussing complex pharmacovigilance topics. This will help you stand out as a strong candidate who can collaborate well with diverse teams.
