Team Leader Data Quality Management (España)

Team Leader Data Quality Management (España)

13 ago
|
Development
|
España

13 ago

Development

España

Summary

Ready to shape the safety of medicines used by millions worldwide?

As a Medical Safety Lead in Cardio Renal Metabolism, you will combine clinical insight and scientific expertise to evaluate safety data, detect signals, and guide critical decisions across the product lifecycle. Working with global cross-functional teams, you will play a pivotal role in helping millions of patients with serious diseases.
About the Role

Location: Barcelona, Spain

Working Model: Hybrid (12 days/month in office )
LI-Hybrid

( Note: this role is also advertised in London, UK. If you are interested in that location, please apply on requisition number 10085146)

Relocation Support: Novartis is unable to offer relocation support - please only apply if the location is accessible to you.

Key accountabilities:
- Monitor clinical safety data, including literature, case reports, and signal detection activities
- Drive the application of AI-enabled solutions to simplify and enhance pharmacovigilance processes, leveraging knowledge of AI agents and their use in medical safety.




- Conduct medical assessment of individual adverse event cases and ensure accurate evaluation
- Identify, evaluate, and monitor safety signals using single-case and aggregate data
- Contribute to responses for regulatory authorities and healthcare professional safety inquiries
- Support preparation of core safety documents, including clinical overviews and summary reports
- Provide medical input to aggregate safety reports and regulatory submissions
- Collaborate cross-functionally to integrate safety insights across integral development teams
- Guide adverse event coding, causality assessment, and interpretation of clinical safety data

Essential Requirements:
- Degree in Pharmacy, Nursing, Pharmacology, Life Sciences, or a medical degree (medical degree required for roles involving medical review of individual case safety reports)
- Fluency in written and spoken English
- At least 3 years’ experience in drug dev

📌 Team Leader Data Quality Management (España)
🏢 Development
📍 España

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