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For Companies At a Glance
- Tasks: Lead Pharmacovigilance activities and manage safety data for innovative biopharmaceutical products.
- Company: Join a global biopharmaceutical company focused on healthcare innovation and sustainability.
- Benefits: Enjoy remote work options and the chance to impact healthcare positively.
- Why this job: Be part of a team dedicated to improving lives through cutting-edge neurological research.
- Qualifications: Life sciences degree with strong experience in Pharmacovigilance and drug safety required.
- Other info: Must reside in the UK and hold a valid UK passport or visa.
The predicted salary is between 43200 - 72000 £ per year.
Job Description
Your new company
My client is a global biopharmaceutical company with a goal of contributing to healthcare innovation and environmental sustainability. They are focused on improving people's quality of life, specialising in neurological diseases. There is an opportunity for a Senior Pharmacovigilance Scientist to join their Pharmacovigilance team.
Inside IR35
Remote working (must be currently living in the UK)
Your new role
As a highly motivated individual, you will serve as a product lead for Pharmacovigilance activities within Safety.
The Senior PV Scientist will lead the signal management process (i.e., signal detection, signal tracking, signal documentation, facilitating decisions regarding signals and safety risk, etc.) for assigned product(s) and evaluate safety data and signals as part of ongoing pharmacovigilance activities. This includes synthesis of data from multiple sources and authoring signal evaluation reports and responding to safety questions from regulatory authorities.You will also lead Aggregate Report management, including strategy, review and finalisation of aggregate safety reports for assigned products, such as PSURs, DSURs, Pharmacovigilance Plans, and Risk Management Plans (RMPs), and authoring safety sections in aggregate reports.
What you'll need to succeed
Life sciences degree.
Strong Pharmacovigilance and drug development foundation, including knowledge of applicable clinical trial safety regulations and post-marketing safety regulations. With several years of hands-on Pharmacovigilance / Drug safety experience in a pharmaceutical company.
Strong experience in authoring aggregate safety reports, safety signal management and responses to regulatory agency requests.
Understands, interprets, analyses, and clearly presents scientific and medical data in verbal and written format
Knowledge of common safety database systems.
Demonstrates leadership and interacts collaboratively and effectively in a team environment, as well as with external colleagues
Applies clinical judgment to interpret case information.
Strong organisational skills, including the ability to prioritise independently with minimal supervision.
Excellence in communication
Strong innovation, decision-making and problem-solving skills
What you need to do now
Before you apply for this position, it is vital that you are in possession of a UK passport or relevant visa to work without restrictions in the UK and residing 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 on 03330106292
Desired Skills and Experience
Pharmacovigilance
Senior Pharmacovigilance Scientist employer: Hays
Contact Detail:
Hays Recruiting Team
StudySmarter Expert Advice 🤫
We think this is how you could land Senior Pharmacovigilance Scientist
✨Tip Number 1
Network with professionals in the pharmacovigilance field. Attend industry conferences, webinars, or local meetups to connect with others who work in similar roles. This can help you gain insights into the company culture and potentially get a referral.
✨Tip Number 2
Familiarise yourself with the latest regulations and guidelines related to pharmacovigilance. Being well-versed in current practices will not only boost your confidence but also demonstrate your commitment to the field during interviews.
✨Tip Number 3
Prepare for potential interview questions by reviewing common scenarios in pharmacovigilance. Think about how you would handle signal detection or respond to regulatory inquiries, as these are key aspects of the role.
✨Tip Number 4
Showcase your leadership skills by discussing past experiences where you led projects or collaborated with teams. Highlighting your ability to work effectively in a team environment will resonate well with the hiring managers.
We think you need these skills to ace Senior Pharmacovigilance Scientist
Some tips for your application 🫡
Tailor Your CV: Make sure your CV highlights your relevant experience in Pharmacovigilance and drug safety. Emphasise your hands-on experience, especially in authoring aggregate safety reports and managing safety signals.
Craft a Compelling Cover Letter: Write a cover letter that showcases your passion for healthcare innovation and your understanding of the role. Mention specific experiences that demonstrate your leadership skills and ability to work collaboratively in a team.
Highlight Relevant Qualifications: Clearly state your life sciences degree and any additional qualifications or certifications related to Pharmacovigilance. This will help you stand out as a qualified candidate.
Showcase Communication Skills: Since strong communication is essential for this role, provide examples of how you've effectively communicated scientific and medical data in previous positions. This could be through presentations, reports, or interactions with regulatory authorities.
How to prepare for a job interview at Hays
✨Showcase Your Expertise
Make sure to highlight your strong foundation in Pharmacovigilance and drug development during the interview. Be prepared to discuss specific experiences where you've successfully managed safety signals or authored aggregate safety reports.
✨Demonstrate Leadership Skills
Since the role requires leadership within the Pharmacovigilance team, share examples of how you've led projects or collaborated effectively with colleagues. This will show your ability to work well in a team environment and take charge when necessary.
✨Prepare for Technical Questions
Expect questions related to clinical trial safety regulations and post-marketing safety regulations. Brush up on your knowledge of safety database systems and be ready to explain how you interpret and present scientific data clearly.
✨Exhibit Strong Communication Skills
Communication is key in this role, so practice articulating your thoughts clearly and concisely. Prepare to discuss how you would respond to safety questions from regulatory authorities, showcasing your ability to convey complex information effectively.
