Senior Pharmacovigilance Scientist

Senior Pharmacovigilance Scientist

Temporary 37 - 50 € / hour (est.) Home office (partial)
Royal Society of Chemistry

At a Glance

  • Tasks: Oversee pharmacovigilance processes and ensure compliance with regulations.
  • Company: Join a leading biopharmaceutical company making a global impact.
  • Benefits: Competitive hourly rate, hybrid work model, and professional growth opportunities.
  • Other info: Dynamic role with potential for career advancement in a supportive environment.
  • Why this job: Make a difference in patient safety while working with industry experts.
  • Qualifications: Strong pharmacovigilance experience and knowledge of international regulations.

The predicted salary is between 37 - 50 € per hour.

Talentmark are recruiting for a Senior Pharmacovigilance Scientist to join a company in the pharmaceutical industry on a contract basis for 12 months. Salary up to £37.76 per hour PAYE, or up to £50.00 per hour Ltd/Umbrella.

Senior Pharmacovigilance Scientist Role

  • Performing oversight of service providers who execute ICSR tasks and Medical Device reports.
  • Acting as a subject matter expert, answering queries and sharing expertise with stakeholders, service providers, business partners, auditors and inspectors.
  • Identifying root causes of non-compliance and agreeing Corrective Actions and Preventative Actions, including implementation where required.
  • Carrying out impact assessments of new or updated regulatory requirements.
  • Supporting regulatory inspection readiness through clear communication of processes, decisions and rationale.

Your Background

  • Strong pharmacovigilance experience, particularly within ICSR case processing.
  • Good knowledge of pharmacovigilance legislation and international regulations, including ICH, EU GVP Modules and FDA requirements.
  • Experience working with service providers, including oversight, relationship management, metrics and analysis.
  • A quality-focused and proactive approach, with experience supporting CAPAs, process improvement and risk mitigation.
  • Medical Device processing experience or knowledge would be desirable.

Company

Our client is one of the world's premier innovative biopharmaceutical companies, discovering, developing and providing over 160 different medicines, vaccines and consumer healthcare products to help improve the lives of millions of people in the UK and around the world every year.

Location

This role is based at our client’s site in Welwyn on a hybrid basis, with 2 days per week onsite.

Apply

For more information, or to apply for this Senior Pharmacovigilance Scientist position, please contact the Key Accounts Team on 01438 870011 or email pharmacontracts@talentmark.co.uk. Please quote reference 187809. It is essential that applicants hold entitlement to work in the UK.

Senior Pharmacovigilance Scientist employer: Royal Society of Chemistry

Join a leading biopharmaceutical company that prioritises innovation and employee development, offering a dynamic work culture where your expertise in pharmacovigilance will be valued. With competitive pay rates and the flexibility of a hybrid working model in Welwyn, you will have the opportunity to contribute to meaningful projects that enhance patient safety while enjoying a supportive environment that fosters professional growth.

Royal Society of Chemistry

Contact Detail:

Royal Society of Chemistry Recruiting Team

StudySmarter Expert Advice🤫

We think this is how you could land Senior Pharmacovigilance Scientist

Tip Number 1

Network like a pro! Reach out to your connections in the pharmaceutical industry, especially those who work 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 ICSR expertise and regulatory knowledge. We recommend practising common interview questions related to pharmacovigilance to showcase your skills confidently.

Tip Number 3

Don’t underestimate the power of follow-ups! After an interview, drop a quick thank-you email to express your appreciation. It keeps you fresh in their minds and shows your enthusiasm for the role.

Tip Number 4

Apply through our website for the best chance at landing that Senior Pharmacovigilance Scientist role. We’ve got all the latest listings, and applying directly can sometimes give you an edge over other candidates!

We think you need these skills to ace Senior Pharmacovigilance Scientist

Pharmacovigilance
ICSR Expertise
Regulatory Compliance
Root Cause Analysis
Corrective Actions and Preventative Actions (CAPAs)
Impact Assessments
Stakeholder Communication

Some tips for your application 🫡

Tailor Your CV:Make sure your CV is tailored to the Senior Pharmacovigilance Scientist role. Highlight your pharmacovigilance experience and any relevant ICSR case processing skills. We want to see how your background aligns with what we're looking for!

Craft a Compelling Cover Letter:Your cover letter is your chance to shine! Use it to explain why you're the perfect fit for this role. Share specific examples of your expertise in pharmacovigilance and how you've tackled challenges in the past. We love a good story!

Showcase Your Knowledge:Don’t forget to mention your understanding of pharmacovigilance legislation and international regulations. We’re keen on candidates who can demonstrate their knowledge of ICH, EU GVP Modules, and FDA requirements. Let us know you’re up to date!

Apply Through Our Website:We encourage you to apply through our website for a smoother process. It helps us keep track of your application and ensures you don’t miss out on any important updates. We can’t wait to hear from you!

How to prepare for a job interview at Royal Society of Chemistry

Know Your Stuff

Make sure you brush up on your pharmacovigilance knowledge, especially around ICSR case processing and relevant regulations like ICH and EU GVP Modules. Being able to discuss these topics confidently will show that you're the right fit for the role.

Showcase Your Experience

Prepare specific examples from your past work where you've successfully managed service providers or implemented CAPAs. This will help demonstrate your hands-on experience and how you can add value to the team.

Ask Smart Questions

Think of insightful questions to ask during the interview about the company's approach to patient safety and regulatory compliance. This shows your genuine interest in the role and helps you assess if the company aligns with your values.

Be Ready for Scenario-Based Questions

Expect to be asked how you would handle certain situations, like identifying root causes of non-compliance. Practising your responses to these types of questions can help you articulate your thought process clearly during the interview.