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For Companies At a Glance
- Tasks: Manage and process safety case reports while ensuring regulatory compliance.
- Company: Join Biomapas & Delta PV, a leader in pharmacovigilance.
- Benefits: Enjoy remote work, monthly bonuses, and an international team.
- Why this job: Make a real impact in drug safety while using your Mandarin skills.
- Qualifications: Bachelor's in Life Sciences and 1 year of pharmacovigilance experience required.
- Other info: Flexible location; work from anywhere while managing multiple cases.
The predicted salary is between 36000 - 60000 £ per year.
Biomapas & Delta PV are looking for a Pharmacovigilance (Case Processing) Specialist with Mandarin language. The Pharmacovigilance Specialist will be responsible for the operational delivery of pharmacovigilance activities at the project level, with a primary focus on safety case intake, processing, and reporting. The role involves end-to-end case processing rather than translation, including medical assessment and regulatory compliance activities.
Responsibilities
- Manage and process end-to-end safety case reports in compliance with global and local regulatory requirements
- Perform triage of incoming safety information, assessing case validity, seriousness, and required follow-up actions
- Review, manage, and archive source documentation in accordance with pharmacovigilance regulations and internal SOPs
- Perform safety database (SDB) data entry, including narrative writing and case documentation
- Conduct medical assessments, including seriousness, causality, and expectedness evaluations
- Assess reporting requirements and ensure timely submission to health authorities and clients
- Perform and document follow-up activities and manage safety-related queries
- Execute quality control checks to ensure data accuracy, completeness, and compliance
- Perform reconciliation activities to ensure consistency across safety databases and source documents
- Prepare line listings and safety reports as required by projects or clients
Requirements
- Bachelor’s degree in Life Sciences field
- Minimum 1 year of experience in pharmacovigilance or safety case processing within the pharmaceutical or CRO industry
- Fluency in Mandarin Chinese (Simplified Chinese) and English, with the ability to process pharmacovigilance safety cases originating in Mandarin, is required
- Hands-on experience with Argus Safety, Veeva Vault or similar safety databases is preferred
- Strong proficiency in MS Office applications
- Ability to work independently while managing multiple cases and deadlines
- Candidates may be based in or outside China; those located in Europe or other regions and willing to work in European working hours are welcome
Benefits
- International team and environment
- Remote/home-based position
- Monthly bonuses
Pharmacovigilance Specialist (Case Processing / Mandarin language) in London employer: Biomapas
Contact Detail:
Biomapas Recruiting Team
StudySmarter Expert Advice 🤫
We think this is how you could land Pharmacovigilance Specialist (Case Processing / Mandarin language) in London
✨Tip Number 1
Network like a pro! Reach out to professionals in the pharmacovigilance field on LinkedIn or at industry events. We can leverage our connections to get insights and maybe even referrals for that Pharmacovigilance Specialist role.
✨Tip Number 2
Prepare for interviews by brushing up on your case processing knowledge. We should be ready to discuss specific scenarios where we've managed safety case reports, as well as our experience with databases like Argus Safety or Veeva Vault.
✨Tip Number 3
Show off your Mandarin skills! If you get the chance, practice discussing pharmacovigilance topics in Mandarin. This will not only boost your confidence but also demonstrate your fluency to potential employers.
✨Tip Number 4
Don’t forget to apply through our website! It’s the best way to ensure your application gets noticed. Plus, we often have insider tips and updates on new roles that might not be advertised elsewhere.
We think you need these skills to ace Pharmacovigilance Specialist (Case Processing / Mandarin language) in London
Some tips for your application 🫡
Tailor Your CV: Make sure your CV highlights your relevant experience in pharmacovigilance and case processing. We want to see how your skills match the job description, so don’t be shy about showcasing your expertise!
Craft a Compelling Cover Letter: Your cover letter is your chance to shine! Use it to explain why you’re passionate about pharmacovigilance and how your Mandarin skills will benefit our team. Keep it engaging and personal – we love to see your personality!
Showcase Your Technical Skills: Mention any hands-on experience you have with safety databases like Argus Safety or Veeva Vault. We’re looking for someone who can hit the ground running, so let us know what tools you’re familiar with!
Apply Through Our Website: We encourage you to apply directly through our website. It’s the best way for us to receive your application and ensures you’re considered for the role. Plus, it’s super easy – just a few clicks and you’re done!
How to prepare for a job interview at Biomapas
✨Know Your Stuff
Make sure you brush up on your pharmacovigilance knowledge, especially around case processing and regulatory compliance. Familiarise yourself with the specific requirements of the role and be ready to discuss how your experience aligns with them.
✨Show Off Your Language Skills
Since fluency in Mandarin is a must, prepare to demonstrate your language skills during the interview. You might be asked to discuss a case or explain a concept in Mandarin, so practice articulating your thoughts clearly in both Mandarin and English.
✨Be Ready for Scenario Questions
Expect scenario-based questions that test your problem-solving skills in pharmacovigilance. Think about past experiences where you had to assess case validity or manage safety-related queries, and be prepared to walk the interviewer through your thought process.
✨Highlight Your Tech Savvy
If you've worked with safety databases like Argus Safety or Veeva Vault, make sure to mention it! Discuss your hands-on experience and how you’ve used these tools to ensure data accuracy and compliance in your previous roles.
