Scientific jobs

Scientific jobs

As a scientific officer at EMA, you will typically be responsible for activities related to human or veterinary medicines in areas such as procedure and scientific management, scientific committee support, pharmacovigilance, and inspections and quality.

You will have obtained a degree in a science field and have proven work experience in the field of medicines regulation from the pharmaceutical industry, a national competent authority or academia. You will have knowledge and understanding of scientific aspects of medicines development, clinical trials methodology, signal detection and pharmacoepidemiology. You will be a curious, solution-driven team player who can communicate verbally and in writing with various audiences.

Search results for "". Page 2 of 2, Results 26 to 32 of 32
Title Deadline for application Type of position
Trainee (Building Retrieval augmented generation system for Clinical trial system users, worldwide) 6 May 2025 23:59 CET Trainee
Trainee (Big Data curriculum on Genomics for the European Medicines Regulatory Network) 6 May 2025 23:59 CET Trainee
Trainee (Analysis of agreement on partial waivers - lessons learnt and impact analysis) 6 May 2025 23:59 CET Trainee
Trainee (Accelerating Innovation, Optimizing Regulation, Strengthening Global Leadership) 6 May 2025 23:59 CET Trainee
Trainee (Vaccine regulatory science)
Trainee (Vaccine regulatory science) 6 May 2025 23:59 CET Trainee
6 May 2025 23:59 CET Trainee
SNE/Epidemiology Specialist
SNE/Epidemiology Specialist 8 April 2025 at 23:59 CEST Seconded National Expert
8 April 2025 at 23:59 CEST Seconded National Expert
SNE/Biostatistician Specialist (evidence generation)
SNE/Biostatistician Specialist (evidence generation) 14 April 2025 at 23:59 CEST Seconded National Expert
14 April 2025 at 23:59 CEST Seconded National Expert

What is it like to work in the Human Medicines Division?

Regulatory Science to 2025 - Shaping the future

 

As science and technology advance and bring potential new treatments and diagnostic tools, regulatory science must advance in tandem so that these can be correctly, rigorously and efficiently assessed. Examples of the transformational research that is having a significant impact on the regulatory science agenda include cell-based therapies, genomics-based diagnostics, drug-device combinations, novel clinical trial design, predictive toxicology, real-world evidence, and ‘big data’ and artificial intelligence.