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- Tasks: Lead Pharmacovigilance activities and manage safety reporting for innovative products.
- Company: Join a leading global pharmaceutical company dedicated to patient safety.
- Benefits: Attractive salary, comprehensive health benefits, and opportunities for professional growth.
- Other info: Dynamic role with a focus on process improvement and cross-functional collaboration.
- Why this job: Make a real difference in drug safety and mentor the next generation of scientists.
- Qualifications: 8-10 years in Pharmacovigilance with strong leadership and analytical skills.
The predicted salary is between 80000 - 100000 £ per year.
As a leader in the Safety Surveillance and Aggregate Reports group of Global Safety Regulatory Sciences (GSRS), the Associate Director is accountable for the oversight and management of Pharmacovigilance activities for an assigned group of products, including:
- Oversight of aggregate reporting for all products within the product group
- Overseeing signal management activities for the assigned group of products
- Oversight of management of responses to ad hoc regulatory responses
- Oversight of literature review/management for safety findings
- Oversight of clinical trial safety activities for assigned products
In this role, the Associate Director may serve as the lead PV Scientist for a group of products as well as manage and mentor PV Scientists, Senior PV Scientists and PV Coordinators assigned to products within the Associate Director’s designated product group. The Associate Director monitors resourcing for all assigned products and manages or reassigns tasks/projects across assigned programs and staff, as workload requires. The Associate Director is responsible for hiring, training, mentoring and managing staff within their group. The Associate Director is responsible for leading initiatives for process improvement, and collaborating with the PV Sciences group, other Safety Staff and cross-functional groups to develop, implement and maintain processes that are compliant with global PV regulations, improve efficiency and lead to consistent work processes across assigned product groups taking into account cross-program practices.
Qualifications
Minimum 8-10 years Pharmacovigilance experience, including experience in aggregate safety reports writing and safety signal management. Minimum of 2 years managing direct reports.
Assoc Director, Drug Safety in Maidenhead employer: Biogen SANDBOX
Contact Detail:
Biogen SANDBOX Recruiting Team
StudySmarter Expert Advice 🤫
We think this is how you could land Assoc Director, Drug Safety in Maidenhead
✨Tip Number 1
Network like a pro! Reach out to your connections in the industry, attend relevant events, and engage with professionals on platforms like LinkedIn. 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 products thoroughly. Understand their values and recent developments in pharmacovigilance. We want you to walk in confident, ready to discuss how your experience aligns with their needs.
✨Tip Number 3
Practice makes perfect! Conduct mock interviews with friends or mentors to refine your answers and get comfortable discussing your experience in drug safety. We’re here to help you shine when it counts!
✨Tip Number 4
Don’t forget to follow up after interviews! A simple thank-you email can go a long way in showing your enthusiasm for the role. And remember, apply through our website for the best chance at landing that Associate Director position!
We think you need these skills to ace Assoc Director, Drug Safety in Maidenhead
Some tips for your application 🫡
Tailor Your CV: Make sure your CV is tailored to the role of Associate Director, Drug Safety. Highlight your relevant experience in Pharmacovigilance and any leadership roles you've held. We want to see how your background aligns with our needs!
Craft a Compelling Cover Letter: Your cover letter is your chance to shine! Use it to explain why you're passionate about drug safety and how your skills can contribute to our team. Keep it engaging and personal – we love to see your personality come through.
Showcase Your Leadership Skills: Since this role involves managing and mentoring staff, be sure to highlight your leadership experience. Share examples of how you've successfully led teams or projects in the past. We’re looking for someone who can inspire and guide others!
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, you’ll find all the details you need about the role and our company culture there!
How to prepare for a job interview at Biogen SANDBOX
✨Know Your Pharmacovigilance Inside Out
Make sure you brush up on your knowledge of pharmacovigilance, especially aggregate safety reports and signal management. Be ready to discuss specific examples from your past experience that demonstrate your expertise in these areas.
✨Showcase Your Leadership Skills
As an Associate Director, you'll be managing a team. Prepare to talk about your leadership style and how you've successfully mentored or managed direct reports in the past. Think of specific instances where you led initiatives for process improvement.
✨Understand the Regulatory Landscape
Familiarise yourself with global pharmacovigilance regulations and compliance requirements. Be prepared to discuss how you've ensured compliance in previous roles and how you would approach this in the new position.
✨Prepare Questions for Them
Interviews are a two-way street! Prepare insightful questions about the company's approach to safety surveillance and how they foster collaboration across teams. This shows your genuine interest in the role and helps you assess if it's the right fit for you.