At a Glance
- Tasks: Lead safety signal management and oversee pharmacovigilance activities for innovative biopharmaceutical products.
- Company: Global biopharmaceutical company focused on healthcare innovation and sustainability.
- Benefits: Competitive pay rates, remote work, and a chance to impact healthcare positively.
- Other info: 12-month contract with opportunities for professional growth in a dynamic environment.
- Why this job: Join a team dedicated to improving lives through cutting-edge drug safety practices.
- Qualifications: Advanced scientific degree and expert experience in pharmacovigilance required.
Your new company is a global biopharmaceutical company focused on healthcare innovation and environmental sustainability, specialising in Oncology, neurology, and rare diseases. They have a position available for a Senior Pharmacovigilance Scientist to join their Pharmacovigilance team on a 12-month initial contract.
Contract Details:
- Remote
- 12 Month + Contract
- INSIDE IR35
- PAYE - Up to £85 p/h (based on experience)
- Umbrella - Up to £109 p/h (based on experience)
Your new role:
As the Senior Pharmacovigilance Scientist, you will serve as a product lead for Pharmacovigilance activities within Safety. The Senior PV Scientist is responsible for overseeing and leading the process for safety signal management activities, writing aggregate reports, responding to safety questions from stakeholders, reviewing medical literature for safety information, and supporting Clinical Trial PV medical activities.
The Senior PV Scientist also serves as a Subject-Matter Expert for Safety and cross-functional teams on relevant global safety regulations and guidelines, data output and analyses, and product-specific information. This role is critical to ensuring products in clinical trials maintain good standing with countries where studies are ongoing and for marketed products, ensuring the marketing authorisation remains in good standing.
What you’ll need to succeed:
- A scientific degree, advanced degree preferred (e.g., M.Sc., PhD, MPH, PharmD).
- Expert experience in the pharmaceutical industry and pharmacovigilance, including safety signal management and writing of aggregate safety reports.
- Strong knowledge of pre- and post-marketing pharmacovigilance legislation.
- Experience with EMA and FDA regulatory submissions.
What you need to do now:
Before applying for this position, it is vital that you possess a UK passport or relevant visa to work without restrictions in the UK and must be based in the UK. If you’re interested in this role, click 'apply now' to forward an up-to-date copy of your CV, or call Roberta Atkins.
Senior Pharmacovigilance Scientist - Signal Management in City of London employer: Hays Life Sciences
Contact Detail:
Hays Life Sciences Recruiting Team
StudySmarter Expert Advice 🤫
We think this is how you could land Senior Pharmacovigilance Scientist - Signal Management in City of London
✨Tip Number 1
Network like a pro! Reach out to your connections in the biopharmaceutical field, especially those in pharmacovigilance. A friendly chat can lead to insider info about job openings or even a referral.
✨Tip Number 2
Prepare for interviews by brushing up on your knowledge of safety signal management and relevant regulations. We recommend practising common interview questions and having examples ready that showcase your expertise in writing aggregate reports.
✨Tip Number 3
Don’t just apply anywhere; focus on companies that align with your values, like those committed to healthcare innovation. Use our website to find roles that excite you and match your skills!
✨Tip Number 4
Follow up after interviews! A quick thank-you email can keep you top of mind. It shows your enthusiasm for the role and gives you another chance to highlight why you're the perfect fit for the Senior Pharmacovigilance Scientist position.
We think you need these skills to ace Senior Pharmacovigilance Scientist - Signal Management in City of London
Some tips for your application 🫡
Tailor Your CV: Make sure your CV is tailored to the Senior Pharmacovigilance Scientist role. Highlight your experience in safety signal management and any relevant aggregate report writing. We want to see how your background aligns with what we're looking for!
Showcase Your Expertise: Don’t hold back on showcasing your expertise in pharmacovigilance legislation and regulatory submissions. Use specific examples from your past roles to demonstrate your knowledge and skills. This will help us see you as a strong candidate!
Be Clear and Concise: When writing your application, keep it clear and concise. Avoid jargon unless it's necessary, and make sure your points are easy to understand. We appreciate straightforward communication that gets to the heart of your qualifications.
Apply Through Our Website: We encourage you to apply through our website for a smoother process. It helps us keep track of applications better and ensures you don’t miss out on any important updates. Plus, it’s super easy!
How to prepare for a job interview at Hays Life Sciences
✨Know Your Stuff
Make sure you brush up on your pharmacovigilance knowledge, especially around safety signal management. Be ready to discuss your experience with aggregate reports like PSURs and DSURs, as well as any relevant regulations like ICH/CIOMS.
✨Showcase Your Expertise
Prepare to highlight your role as a Subject-Matter Expert. Think of examples where you've led safety signal management activities or contributed to regulatory submissions. This will demonstrate your capability and confidence in the field.
✨Understand the Company’s Mission
Familiarise yourself with the company’s focus on healthcare innovation and environmental sustainability. Be prepared to discuss how your values align with theirs and how you can contribute to improving people's quality of life through your work.
✨Ask Insightful Questions
Prepare thoughtful questions about the team dynamics, ongoing projects, and the company's approach to pharmacovigilance. This shows your genuine interest in the role and helps you assess if it’s the right fit for you.