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- Tasks: Support safety surveillance in early development oncology and immune-oncology.
- Company: Global biopharmaceutical company focused on healthcare innovation and sustainability.
- Benefits: Hybrid work model, competitive contract terms, and opportunity to impact patient safety.
- Why this job: Join a team making a difference in oncology and contribute to groundbreaking research.
- Qualifications: Scientific degree required; expertise in pharmacovigilance and oncology preferred.
- Other info: 6-month contract with potential for growth in a dynamic environment.
The predicted salary is between 60000 - 80000 £ per year.
Your new company My client, a global biopharmaceutical company with a goal of contributing to healthcare innovation and environmental sustainability and which is focused on improving people's quality of life, specialising in Oncology, neurology and rare diseases, has a position available for a Clinical Pharmacovigilance Scientist to join their Global Patient Safety team on a 6-month initial contract within their early development oncology / immune-oncology arena. Hybrid - 1 day per week in London 6 Month + Contract OUTSIDE IR35
Your new role As the Global Clinical Pharmacovigilance Scientist, you will support the Global Patient Safety (GPS) early development oncology (specifically FIH) / immune-oncology Therapy Area through safety surveillance activities, including scientific analyses, case reviews, literature reviews, data assessment, signal management, and risk assessment, evaluation of product quality issues and emerging safety issues, including contribution to safety documents, aggregate reports, (d)RMPs and responses to health authority requests, submission, interactions etc. for allocated assets/products, projects and activities. Support definition of safety strategy for FIH (First in Human) trials and work with the safety physician on the IND/CTA enabling documents. Interact with vendors, CROs and business partners as stipulated in the SDEA, evaluation of product quality issues and the overall safety strategy.
What you’ll need to succeed In order to apply for the Global Clinical Pharmacovigilance Scientist role, you must possess:
- A scientific degree, advanced degree preferred (e.g., MSc, PhD, MPH, PharmD).
- Expert experience of pharmaceutical industry and pharmacovigilance, including aggregate report writing and signal management.
- Expert experience of early development oncology (specifically FIH) or/and immune oncology.
- Strong knowledge of pre- and post‑marketing pharmacovigilance legislation (CTR, GVP Modules, ICH/CIOMS).
- Experience with EMA and FDA regulatory submissions.
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 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 on (phone number removed).
Clinical Pharmacovigilance Scientist - Oncology employer: Hays Life Sciences
Contact Detail:
Hays Life Sciences Recruiting Team
StudySmarter Expert Advice 🤫
We think this is how you could land Clinical Pharmacovigilance Scientist - Oncology
✨Tip Number 1
Network like a pro! Reach out to professionals in the oncology and pharmacovigilance fields on LinkedIn. Join relevant groups, participate in discussions, and don’t be shy about asking for informational interviews. We all know that sometimes it’s not just what you know, but who you know!
✨Tip Number 2
Prepare for those interviews! Research the company and its recent projects in oncology and immune-oncology. We recommend practising common interview questions and tailoring your answers to highlight your expertise in pharmacovigilance. Show them you’re the perfect fit for their Global Patient Safety team!
✨Tip Number 3
Follow up after interviews! A quick thank-you email can go a long way. It shows your enthusiasm for the role and keeps you fresh in their minds. We suggest mentioning something specific from the interview to make it personal.
✨Tip Number 4
Don’t forget to apply through our website! We’ve got loads of opportunities that might just be the perfect match for your skills. Plus, applying directly can sometimes give you an edge over other candidates. Let’s get you that job!
We think you need these skills to ace Clinical Pharmacovigilance Scientist - Oncology
Some tips for your application 🫡
Tailor Your CV: Make sure your CV is tailored to the Clinical Pharmacovigilance Scientist role. Highlight your relevant experience in oncology and pharmacovigilance, and don’t forget to mention any specific projects or achievements that align with the job description.
Craft a Compelling Cover Letter: Your cover letter is your chance to shine! Use it to explain why you’re passionate about this role and how your background makes you a perfect fit. Be sure to mention your understanding of FIH trials and any relevant regulatory experience.
Showcase Your Skills: In your application, clearly showcase your skills in safety surveillance activities, data assessment, and signal management. Use examples from your past work to demonstrate your expertise and how you can contribute to the Global Patient Safety team.
Apply Through Our Website: We encourage you to apply through our website for a smoother application process. It’s the best way to ensure your application gets the attention it deserves, so don’t hesitate to click that 'apply now' button!
How to prepare for a job interview at Hays Life Sciences
✨Know Your Stuff
Make sure you brush up on your knowledge of pharmacovigilance, especially in oncology and immune-oncology. Familiarise yourself with the latest regulations and guidelines from EMA and FDA, as well as any recent developments in early-stage clinical trials.
✨Showcase Your Experience
Prepare to discuss your previous roles in detail, particularly your experience with aggregate report writing and signal management. Be ready to provide specific examples of how you've contributed to safety strategies or handled product quality issues in past positions.
✨Ask Smart Questions
Think of insightful questions to ask during the interview. This could be about the company's approach to safety surveillance or how they handle interactions with CROs and vendors. It shows you're genuinely interested and have done your homework.
✨Be Ready for Scenario-Based Questions
Expect to face scenario-based questions that assess your problem-solving skills in pharmacovigilance. Practice articulating your thought process clearly, as this will demonstrate your analytical abilities and how you approach risk assessment.