At a Glance
- Tasks: Support drug safety operations and ensure patient safety in a dynamic environment.
- Company: Leading pharmaceutical company dedicated to innovative treatments and patient care.
- Benefits: Competitive salary, health benefits, and opportunities for professional growth.
- Other info: Collaborative team culture with opportunities for international projects.
- Why this job: Make a real difference in patients' lives while working with cutting-edge drug safety practices.
- Qualifications: Passion for pharmacovigilance and relevant experience in the pharmaceutical industry.
The predicted salary is between 35000 - 45000 £ 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 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.
Drug Safety Operations Associate - UK & Nordics in Maidenhead employer: Grünenthal
As a Drug Safety Operations Associate in Maidenhead, you will be part of a dynamic team dedicated to improving patient lives through innovative medicines. Our company fosters a collaborative and inclusive work culture, offering extensive training and development opportunities to help you grow in your career. With a commitment to excellence and a focus on patient safety, we provide a supportive environment where your contributions truly make a difference.
StudySmarter Expert Advice🤫
We think this is how you could land Drug Safety Operations Associate - UK & 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. We can’t stress enough how valuable personal connections can be in landing that dream job.
✨Tip Number 2
Prepare for interviews by researching the company and its drug safety operations. We recommend practising common interview questions and tailoring your answers to highlight your passion for pharmacovigilance.
✨Tip Number 3
Showcase your skills! Bring along examples of your work or projects related to drug safety during interviews. We love seeing how you’ve applied your knowledge in real-world scenarios.
✨Tip Number 4
Don’t forget to apply through our website! It’s the best way to ensure your application gets noticed. We’re always on the lookout for passionate individuals ready to make a difference in drug safety.
We think you need these skills to ace Drug Safety Operations Associate - UK & Nordics in Maidenhead
Some tips for your application 🫡
Tailor Your CV:Make sure your CV is tailored to the Drug Safety Operations Associate 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. Be genuine and let us know why you’re excited about this opportunity at StudySmarter.
Showcase Your Skills:Don’t forget to showcase your language skills and IT competence, especially if you have experience with Microsoft tools. We value proactive and solution-oriented individuals, so make sure to highlight those traits in your application.
Apply Through Our Website:We encourage you to apply through our website for a smoother process. It’s the best way for us to receive your application and get you on our radar. Let’s make a difference together!
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 and Nordics. 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 problems or improved processes in previous roles. Highlighting your solution-oriented mindset will resonate well with the interviewers, especially in a high-stakes environment like drug safety.
✨Demonstrate Team Collaboration
Since this role involves working within an international matrix, be ready to share experiences where you've successfully collaborated with diverse teams. Emphasise your ability to communicate effectively and work towards common goals, as this is crucial in a global drug safety context.
✨Ask Insightful Questions
Prepare thoughtful questions about the company's approach to drug safety and how they handle challenges in pharmacovigilance. This not only shows your interest in the role but also helps you gauge if the company aligns with your values and career aspirations.
