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 do 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 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 Thatcham employer: Job Search Place Limited
As an Associate Drug Safety Manager, you'll 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 growth, offering you the chance to work alongside talented professionals while contributing to meaningful projects. With a strong commitment to employee development and a culture that values proactive solutions, we provide a rewarding workplace where your passion for pharmacovigilance can truly make a difference.
StudySmarter Expert Advice🤫
We think this is how you could land Associate Drug Safety Manager (UK, Ireland, Nordics) in Thatcham
✨Tip Number 1
Network like a pro! Reach out to professionals in the drug safety field on LinkedIn or at industry events. We can’t stress enough how valuable personal connections can be in landing that Associate Drug Safety Manager role.
✨Tip Number 2
Prepare for interviews by researching the company’s recent projects and their impact on patient safety. We want you to show your passion for pharmacovigilance and how you can contribute to their mission of making a positive difference.
✨Tip Number 3
Practice common interview questions related to drug safety operations. We suggest doing mock interviews with friends or mentors to boost your confidence and refine your answers.
✨Tip Number 4
Don’t forget to apply through our website! It’s the best way to ensure your application gets noticed. 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 Thatcham
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 at StudySmarter. Keep it engaging and personal, showing us why you're the perfect fit.
Showcase Your Skills:Don’t forget to highlight 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 directly through our website. It’s the best way for us to receive your application and ensures you’re considered for the role. Plus, it’s super easy to do!
How to prepare for a job interview at Job Search Place Limited
✨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 how they fit into the global context. This will show your passion for the field and your readiness to contribute.
✨Showcase Your Problem-Solving Skills
Be prepared to discuss specific examples where you've proactively solved issues in a drug safety or pharmacovigilance setting. Think about times when you had to manage deviations or implement CAPA measures, and be ready to explain your thought process and outcomes.
✨Demonstrate Team Collaboration
Since this role involves working within an international matrix environment, highlight your experience collaborating with diverse teams. Share stories that illustrate your ability to work effectively with colleagues from different backgrounds and how you’ve contributed to a high-performing team.
✨Prepare Questions About the Role
Have insightful questions ready about the company's approach to drug safety and how they support their employees in maintaining a patient-centric focus. This not only shows your interest but also helps you gauge if the company aligns with your values and career goals.
