At a Glance
- Tasks: Oversee ICSR tasks and ensure compliance in pharmacovigilance operations.
- Company: Join a leading biopharmaceutical company making a global impact.
- Benefits: Competitive pay, hybrid work model, and opportunities for professional growth.
- Other info: Dynamic role with a focus on quality and process improvement.
- Why this job: Make a difference in patient safety while working with top industry experts.
- Qualifications: Strong pharmacovigilance experience and knowledge of international regulations required.
The predicted salary is between 75000 - 104000 £ per year.
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.
It is essential that applicants hold entitlement to work in the UK.
Senior PV Scientist — ICSR & Compliance (Hybrid, 12m) in Welwyn employer: Talentmark
As a leading biopharmaceutical company, we pride ourselves on fostering a collaborative and innovative work environment that empowers our employees to make a meaningful impact in patient safety. With competitive pay rates and a hybrid working model based in Welwyn, we offer excellent opportunities for professional growth, continuous learning, and the chance to contribute to life-changing healthcare solutions. Join us to be part of a team that values expertise, encourages proactive problem-solving, and is dedicated to improving lives globally.
StudySmarter Expert Advice🤫
We think this is how you could land Senior PV Scientist — ICSR & Compliance (Hybrid, 12m) in Welwyn
✨Tip Number 1
Network like a pro! Reach out to your connections in the pharmaceutical industry and let them know you're on the lookout for opportunities. You never know who might have a lead or can put in a good word for you.
✨Tip Number 2
Prepare for interviews by brushing up on your pharmacovigilance knowledge. Be ready to discuss ICSR case processing and compliance issues, as these will likely come up. We recommend practising common interview questions with a friend or using mock interview tools.
✨Tip Number 3
Showcase your expertise! When you get the chance to speak with potential employers, highlight your experience with service providers and your proactive approach to quality and compliance. This is your moment to shine!
✨Tip Number 4
Don't forget to apply through our website! It’s the best way to ensure your application gets noticed. Plus, we’re always looking for talented individuals like you to join our team in making a difference in patient safety.
We think you need these skills to ace Senior PV Scientist — ICSR & Compliance (Hybrid, 12m) in Welwyn
Some tips for your application 🫡
Tailor Your CV:Make sure your CV is tailored to the Senior Pharmacovigilance Scientist role. Highlight your relevant experience in ICSR case processing and any specific projects that showcase your expertise in pharmacovigilance legislation.
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. Mention your experience with service providers and how you've contributed to compliance and process improvements in past roles.
Showcase Your Expertise:Don’t shy away from showcasing your knowledge of international regulations like ICH and EU GVP Modules. We want to see how your background aligns with the responsibilities outlined in the job description.
Apply Through Our Website:For the best chance of success, make sure to apply through our website. It’s the easiest way for us to receive your application and get you one step closer to joining our team!
How to prepare for a job interview at Talentmark
✨Know Your Pharmacovigilance 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 Oversight Experience
Prepare examples of how you've managed service providers in the past. Talk about your relationship management skills and how you've ensured compliance. This will demonstrate your ability to oversee ICSR tasks effectively.
✨Be Ready for Compliance Questions
Expect questions about identifying root causes of non-compliance and how you've implemented Corrective Actions and Preventative Actions (CAPAs). Have specific examples ready to illustrate your proactive approach to quality and risk mitigation.
✨Communicate Clearly
Since supporting regulatory inspection readiness is key, practice articulating your thought processes and decisions clearly. This will help you convey your expertise effectively to stakeholders and auditors during the interview.
