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 in Maidenhead employer: Grünenthal
As an Associate Drug Safety Manager at our Maidenhead location, you will be part of a dynamic team dedicated to advancing patient safety and innovative treatment options. We pride ourselves on fostering a collaborative work culture that encourages professional growth and development, offering comprehensive training and support to help you excel in your role. With a commitment to making a positive impact on lives, our state-of-the-art facilities and focus on employee well-being make us an exceptional employer in the pharmaceutical industry.
StudySmarter Expert Advice🤫
We think this is how you could land Associate Drug Safety Manager in Maidenhead
✨Tip Number 1
Network like a pro! Reach out to professionals in the drug safety field on LinkedIn or at industry events. We all know that sometimes it’s not just what you know, but who you know that can help you land that dream job.
✨Tip Number 2
Prepare for interviews by researching the company and its drug safety initiatives. We recommend practising common interview questions and tailoring your answers to highlight your passion for pharmacovigilance and patient safety.
✨Tip Number 3
Showcase your skills! Bring along examples of your previous work or projects related to pharmacovigilance. We want to see how you’ve contributed to maintaining safety profiles and compliance in past roles.
✨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 genuinely interested in joining our mission to change lives for the better.
We think you need these skills to ace Associate Drug Safety Manager in Maidenhead
Some tips for your application 🫡
Tailor Your CV:Make sure your CV reflects the skills and experiences that match the Associate Drug Safety Manager role. Highlight any relevant pharmacovigilance experience and your passion for patient safety to catch our eye!
Craft a Compelling Cover Letter:Your cover letter is your chance to shine! Share why you're excited about this role and how your background aligns with our mission of improving lives through innovative medicines. Keep it personal and engaging!
Showcase Your Skills:Don’t forget to mention your language skills and IT competence, especially if you have experience with Microsoft tools. We love proactive and solution-oriented candidates, so let us know how you've demonstrated these traits in your past roles.
Apply Through Our Website:We encourage you to apply directly through our website. It’s the best way to ensure your application gets into the right hands. Plus, it shows you’re serious about joining our team at StudySmarter!
How to prepare for a job interview at Grünenthal
✨Know Your Pharmacovigilance Basics
Make sure you brush up on your pharmacovigilance knowledge before the interview. Understand the local regulations and how they apply to drug safety operations in the UK, Ireland, and Nordics. This will show that you're not just passionate about the role but also well-informed.
✨Showcase Your Problem-Solving Skills
Be prepared to discuss specific examples where you've proactively solved issues in a pharmacovigilance context. Think of situations where you had to manage safety information or handle audits. This will demonstrate your solution-oriented mindset, which is crucial for this role.
✨Highlight Your Teamwork Experience
Since this role involves collaboration within an international matrix, share experiences where you've successfully worked in teams. Emphasise your ability to communicate effectively with colleagues from different backgrounds, especially in a high-pressure environment.
✨Prepare Questions About the Company Culture
Research the company’s values and culture, and prepare thoughtful questions to ask during the interview. This shows your genuine interest in the organisation and helps you assess if it’s the right fit for you. Plus, it gives you a chance to engage with the interviewers on a deeper level.
