Find a job 
Featured Companies 
Featured Universities 
For Companies At a Glance
- Tasks: Review and ensure high-quality documents in pharmacovigilance for innovative healthcare solutions.
- Company: Leading biopharmaceutical company focused on healthcare innovation and sustainability.
- Benefits: Hybrid work model, competitive pay, and opportunities for professional growth.
- Why this job: Join a team making a real impact in healthcare while developing your skills.
- Qualifications: Degree in life sciences, writing experience in pharma, and familiarity with drug safety regulations.
- Other info: Dynamic role with potential for career advancement in a supportive environment.
The predicted salary is between 40000 - 50000 £ per year.
Your new company is a leading 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 Oncology, neurology, rare diseases, ophthalmology and immunology. There is an opportunity for a Pharmacovigilance Quality Document Associate to join their Quality Document Review team on an initial 12-month contract.
Your new role involves performing QC (quality review) to ensure documents authored by the Safety Surveillance and Aggregate Reports (SSA) team or their vendors are of high quality; supporting process improvement and other SSA functions (e.g., vendor management, SharePoint management).
- Source data verification to ensure that all data and methods in all assigned documents agree with source documents, including checking text against database outputs.
- Editorial, technical, and scientific reviews for grammatical and stylistic consistency and accuracy.
- Provide document findings so that appropriate actions can be taken by authors.
What you’ll need to succeed:
- Hold a university degree in a life science or Healthcare.
- Writing and editing experience within the pharmaceutical or biotech industry - medical writing, scientific editing and/or publishing.
- Familiarity with Pharmacovigilance and drug development, including knowledge of applicable clinical trial safety regulations and post-marketing safety regulations.
- Exceptional English writing skills, comfortable with medical terminology, and the American Medical Association Manual of Style.
- Skilled with common data processing software (Excel, Pivot tables, PowerPoint, Microsoft Word, Business Objects).
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 living 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.
Pharmacovigilance Quality Document Reviewer employer: Hays Life Sciences
Contact Detail:
Hays Life Sciences Recruiting Team
StudySmarter Expert Advice 🤫
We think this is how you could land Pharmacovigilance Quality Document Reviewer
✨Tip Number 1
Network like a pro! Reach out to people in the biopharmaceutical industry, especially those working 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 knowledge of drug development and safety regulations. We recommend practising common interview questions related to quality document review to show you're the right fit for the role.
✨Tip Number 3
Showcase your writing skills! Bring samples of your medical writing or editing work to interviews. This will demonstrate your expertise and give you an edge over other candidates.
✨Tip Number 4
Don't forget to apply through our website! It’s the best way to ensure your application gets noticed. Plus, we love seeing candidates who are proactive about their job search.
We think you need these skills to ace Pharmacovigilance Quality Document Reviewer
Some tips for your application 🫡
Tailor Your CV: Make sure your CV is tailored to the Pharmacovigilance Quality Document Reviewer role. Highlight your relevant experience in medical writing and editing, especially within the pharmaceutical or biotech industry. We want to see how your skills align with what we're looking for!
Showcase Your Skills: Don’t forget to showcase your exceptional English writing skills and familiarity with medical terminology. Include examples of your work that demonstrate your ability to present scientific data clearly and accurately. This will help us see your potential fit for the team!
Be Clear and Concise: When writing your application, be clear and concise. Use straightforward language and avoid jargon unless necessary. We appreciate a well-structured application that gets straight to the point, so make it easy for us to see your qualifications!
Apply Through Our Website: Finally, make sure to apply through our website! It’s the best way for us to receive your application and ensures you’re considered for the role. We can’t wait to see what you bring to the table!
How to prepare for a job interview at Hays Life Sciences
✨Know Your Stuff
Make sure you brush up on your knowledge of pharmacovigilance and drug development. Familiarise yourself with the latest regulations and guidelines, especially those related to clinical trial safety and post-marketing safety. This will show that you're not just a candidate, but someone who genuinely understands the field.
✨Showcase Your Writing Skills
Since exceptional writing skills are crucial for this role, prepare to discuss your previous writing and editing experiences. Bring examples of your work, whether it's medical writing or scientific editing, and be ready to explain how you ensure clarity and accuracy in your documents.
✨Be Detail-Oriented
As a Quality Document Reviewer, attention to detail is key. During the interview, highlight instances where your meticulous nature has led to successful outcomes. Discuss how you approach source data verification and document reviews to ensure high-quality outputs.
✨Familiarise with Tools
Get comfortable with the common data processing software mentioned in the job description, like Excel and Microsoft Word. If you can, practice using features like Pivot tables or formatting styles that align with the American Medical Association Manual of Style. Being tech-savvy will give you an edge!