Senior Pharmacovigilance Scientist
Senior Pharmacovigilance Scientist

Senior Pharmacovigilance Scientist

Full-Time 43200 - 72000 £ / year (est.) No home office possible
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At a Glance

  • Tasks: Lead Pharmacovigilance activities, manage safety signals, and author safety reports.
  • 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 improving lives through innovative solutions in neurological diseases.
  • Qualifications: Life sciences degree with strong experience in Pharmacovigilance and drug safety.
  • Other info: Must reside in the UK and hold a UK passport or relevant visa.

The predicted salary is between 43200 - 72000 £ per year.

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 IR35Remote 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 formatKnowledge of common safety database systems.Demonstrates leadership and interacts collaboratively and effectively in a team environment, as well as with external colleaguesApplies clinical judgment to interpret case information.Strong organisational skills, including the ability to prioritise independently with minimal supervision.Excellence in communicationStrong innovation, decision-making and problem-solving skillsWhat 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 03330106292Desired Skills and ExperiencePharmacovigilance

Senior Pharmacovigilance Scientist employer: LinkedIn

Join a leading global biopharmaceutical company that prioritises healthcare innovation and environmental sustainability, offering a dynamic work culture that fosters collaboration and professional growth. As a Senior Pharmacovigilance Scientist, you will play a crucial role in enhancing patient safety while enjoying the flexibility of remote working from the UK, alongside opportunities for continuous learning and development in a supportive environment dedicated to improving lives.
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Contact Detail:

LinkedIn Recruiting Team

StudySmarter Expert Advice 🤫

We think this is how you could land Senior Pharmacovigilance Scientist

✨Tip Number 1

Familiarise yourself with the latest pharmacovigilance regulations and guidelines. This will not only help you in interviews but also demonstrate your commitment to staying updated in a rapidly evolving field.

✨Tip Number 2

Network with professionals in the pharmacovigilance community. Attend relevant webinars or conferences, and connect with industry experts on platforms like LinkedIn to gain insights and potentially get referrals.

✨Tip Number 3

Prepare to discuss specific case studies or experiences where you've successfully managed safety signals or authored aggregate reports. Real-life examples can set you apart from other candidates.

✨Tip Number 4

Research the company’s recent projects and contributions to healthcare innovation. Being knowledgeable about their work will show your genuine interest and help you tailor your discussions during the interview.

We think you need these skills to ace Senior Pharmacovigilance Scientist

Pharmacovigilance Expertise
Signal Management
Aggregate Report Management
Knowledge of Clinical Trial Safety Regulations
Post-Marketing Safety Regulations
Data Synthesis and Analysis
Authoring Safety Reports
Regulatory Agency Communication
Leadership Skills
Team Collaboration
Clinical Judgment
Organisational Skills
Prioritisation Skills
Effective Communication
Innovation and Problem-Solving Skills

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 LinkedIn

✨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 that you can take charge and work well in a team environment.

✨Prepare for Technical Questions

Expect questions related to clinical trial safety regulations and post-marketing safety regulations. Brush up on your knowledge of these areas and be ready to explain how you've applied this knowledge in your previous roles.

✨Communicate Clearly

Given the importance of communication in this role, practice articulating complex scientific and medical data clearly and concisely. This will demonstrate your ability to present information effectively to both technical and non-technical audiences.

Senior Pharmacovigilance Scientist
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  • Senior Pharmacovigilance Scientist

    Full-Time
    43200 - 72000 £ / year (est.)

    Application deadline: 2027-08-13

  • L

    LinkedIn

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