At a Glance
- Tasks: Lead global patient safety case processing and ensure compliance with regulations.
- Company: Join Regeneron, a science-driven company making a difference in patients' lives.
- Benefits: Competitive salary, bonuses, health benefits, and flexible working options.
- Other info: Inclusive workplace culture with excellent career development opportunities.
- Why this job: Make a real impact in the pharmaceutical industry while growing your career.
- Qualifications: 10 years of experience in pharmacovigilance and strong leadership skills required.
The predicted salary is between 70000 - 90000 £ per year.
At Regeneron, we use science and innovation to develop life-changing medicines for people with serious diseases. We are seeking an Associate Director, PV Case Operations to join our Global Patient Safety team, supporting case processing across global development and commercial programmes in a hybrid work mode. In this role, you will lead vendor oversight, Individual Case Safety Report (ICSR) quality governance, and inspection readiness while collaborating with vendor teams, internal partners, license partners, auditors, and Health Authority inspectors. This position offers the opportunity to contribute to a fast-growing, science-driven organization making a meaningful difference to patients worldwide.
Discover your role:
- Own accurate, timely case processing across global development and marketed products, per applicable regulations and Regeneron SOPs.
- Lead vendor oversight for end-to-end ICSR receipt, processing, distribution, and submission.
- Own ICSR quality standards covering narrative, case validity, and source document reconciliation.
- Establish tiered quality review frameworks aligned to case complexity, risk, and product lifecycle stage.
- Monitor submission timelines and vendor SLAs, maintain inspection readiness, and respond to audit findings.
- Lead root cause analysis and own CAPAs through closure and effectiveness checks.
- Evaluate AI-enabled tools for data ingestion, workflow automation, and metrics.
- You mentor staff and communicate clearly with senior management and partners.
This role requires:
- Pharmacy, nursing, or equivalent degree required; advanced degree preferred.
- Typically 10 years of Pharmacovigilance, Drug Safety, or PV Quality experience in pharma or biotech.
- Well-informed on FDA, EU, and ICH guidelines governing pharmacovigilance for clinical trial and post-marketing environments.
- Experience managing teams on complex, cross-functional projects.
- Proven ability to deliver organisational projects through individual contributors or other managers.
- Strong communication and partner management skills, with ability to resolve and escalate complex issues.
We are committed to building a workplace with an inclusive culture. Regeneron is an equal opportunity employer and all qualified applicants will receive consideration for employment without regard to race, colour, religion or belief (or lack thereof), sex, sexual orientation, gender identity or expression, gender reassignment, marital or civil partnership status, civil status, pregnancy or parental status, age, disability, nationality, citizenship status, ethnic or national origin, membership of the Traveler community, familial status, genetic information, military or veteran status, or any other characteristic protected under applicable law.
Where required, we will provide reasonable accommodation to applicants with known disabilities or chronic illnesses during the recruitment process, unless such accommodation would impose undue hardship.
Regeneron offers a competitive and comprehensive total rewards package which may include, depending on country and role: annual bonuses or other incentive plans, equity awards, pension or retirement benefits, health and wellness programs, fitness centers, insurance benefits (e.g. medical, dental, vision, life and disability), paid time off, and family support benefits.
Associate Director Global Patient Safety in Uxbridge employer: Regeneron Pharmaceuticals
At Regeneron, we pride ourselves on being an exceptional employer, offering a dynamic and inclusive work culture that fosters innovation and collaboration. Located in Uxbridge, UK, our hybrid work model allows for flexibility while contributing to life-changing medicines that make a real difference in patients' lives. With comprehensive benefits, opportunities for professional growth, and a commitment to employee well-being, Regeneron is the ideal place for passionate individuals looking to advance their careers in the pharmaceutical industry.
StudySmarter Expert Advice🤫
We think this is how you could land Associate Director Global Patient Safety in Uxbridge
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We think you need these skills to ace Associate Director Global Patient Safety in Uxbridge
Some tips for your application 🫡
Showcase Your Relevant Experience:When applying for a role in the pharmaceutical industry, it's crucial to highlight any relevant experience you have. Whether that's internships, lab work, or even related coursework, make sure to weave this into your CV and cover letter. We want to see how your background aligns with the role you're applying for at Regeneron Pharmaceuticals!
Emphasise Your Understanding of Regulations:The pharmaceutical industry is heavily regulated, so it's important to indicate your familiarity with industry standards and regulations. In your cover letter, mention any training or certifications you've received that are relevant, or discuss projects where you’ve navigated compliance. This will show Regeneron Pharmaceuticals that you're not just a fit for the job but also a safety-conscious candidate!
Tailor Your CV to Be Result-Driven:Craft your CV to highlight quantifiable achievements, especially if you have previous roles in pharmaceuticals or related fields. Use metrics to demonstrate your impact, such as improved processing times or successful project completions while working on trials. This analytical approach will resonate well with hiring managers at Regeneron Pharmaceuticals!
Convey Your Passion for the Industry:In your cover letter, express why you are passionate about working in the pharmaceutical sector. Whether it’s your desire to contribute to groundbreaking drug research or improve patient outcomes, let it shine through! At Regeneron Pharmaceuticals, we value candidates who are truly enthusiastic about their work—you might just stand out from the crowd.
How to prepare for a job interview at Regeneron Pharmaceuticals
✨Understand the Science
Make sure you brush up on key pharmaceutical concepts and recent developments in the industry. You might get asked some technical questions during the interview at Regeneron Pharmaceuticals that show your grasp of drug development processes or regulatory requirements, so be ready to discuss them clearly.
✨Showcase Relevant Experience
If you have any hands-on experience or internships in a laboratory setting, be sure to highlight these in your responses. Think about the projects you worked on, the methodologies you used, and the impact you made. It's all about telling a story that connects your background to the role you're applying for.
✨Know Their Products
Take some time to familiarise yourself with Regeneron Pharmaceuticals’s product range and recent breakthroughs. Understanding their portfolio not only shows your enthusiasm for the role but also allows you to ask insightful questions that demonstrate your interest in actively contributing to their projects.
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In a full-time pharmaceutical role, understanding the regulatory landscape is crucial. Prepare for situational questions that may test your problem-solving skills concerning compliance and safety standards. You could be asked how you'd handle a hypothetical issue regarding a drug’s market release, so think through your approach.