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 international collaboration opportunities.
- 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 a 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 oriented 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: Gr?nenthal GmbH
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 collaboration and professional growth, offering opportunities for continuous learning and development in the pharmaceutical industry. With a strong commitment to employee well-being and a culture that values passion and dedication, we provide a rewarding workplace where your contributions truly make a difference.
StudySmarter Expert Advice🤫
We think this is how you could land Associate Drug Safety Manager (UK, Ireland, Nordics) in Maidenhead
✨Network Like a Pro
Get out there and connect with people in the industry! Attend events, join online forums, or even hit up LinkedIn. The more you engage with professionals in drug safety, the better your chances of landing that Associate Drug Safety Manager role.
✨Show Off Your Skills
When you get the chance to chat with potential employers, make sure to highlight your relevant experience and skills. Talk about your understanding of pharmacovigilance operations and how you can contribute to a high-performing system. We want to see your passion shine through!
✨Prepare for Interviews
Do your homework before interviews! Research the company’s recent projects and their impact on patient safety. Be ready to discuss how you can support their mission and bring innovative ideas to the table. Confidence is key, so practice makes perfect!
✨Apply Through Our Website
Don’t forget to apply directly through our website! It’s the best way to ensure your application gets noticed. Plus, we love seeing candidates who are proactive and eager to join our team in making a difference in drug safety.
We think you need these skills to ace Associate Drug Safety Manager (UK, Ireland, Nordics) in Maidenhead
Some tips for your application 🫡
Tailor Your CV:Make sure your CV is tailored to the Associate Drug Safety Manager role. Highlight relevant experience in pharmacovigilance and any specific skills that match the job description. We want to see how you can contribute to our mission!
Craft a Compelling Cover Letter:Your cover letter is your chance to shine! Use it to express your passion for drug safety and how your background aligns with our goals. Keep it engaging and personal, so we get a sense of who you are.
Showcase Your Skills:Don’t forget to showcase your language skills and IT competence. If you have experience with Microsoft tools or any other relevant software, let us know! We love seeing candidates who are proactive and solution-oriented.
Apply Through Our Website:We encourage you to apply through our website for the best chance of getting noticed. It’s straightforward and ensures your application goes directly to us. We can’t wait to see what you bring to the table!
How to prepare for a job interview at Gr?nenthal GmbH
✨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 this will show your commitment to patient safety and compliance during the interview.
✨Showcase Your Problem-Solving Skills
Be prepared to discuss specific examples where you've proactively solved issues in a drug safety context. Highlighting your ability to manage deviations or implement CAPA measures will demonstrate your readiness for the challenges of the role.
✨Familiarise Yourself with the Company’s Vision
Research the company’s mission and recent developments in drug safety. Being able to articulate how your values align with their vision of improving patient lives will set you apart from other candidates.
✨Prepare Questions About the Role
Think of insightful questions to ask about the local pharmacovigilance system and how it integrates with global operations. This shows your genuine interest in the position and helps you assess if it's the right fit for you.
