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 1 of 2, Results 1 to 25 of 33
Title Deadline for application Type of position
SNE/Scientific Specialist (quality of pharmaceutical veterinary medicinal products) 12 June 2023 at 23:59 CET Seconded National Expert
Trainee (Patients' involvement in referral procedures) 18 June 2023 23:59 CET Trainee
Trainee (Small and Medium-sized Enterprises Office) 18 June 2023 23:59 CET Trainee
Trainee (Product reporting)
Trainee (Product reporting) 18 June 2023 23:59 CET Trainee
18 June 2023 23:59 CET Trainee
Pharmacoepidemiology Specialist
Pharmacoepidemiology Specialist 30 June 2023 at 23.59 CET Temporary agent
30 June 2023 at 23.59 CET Temporary agent
Trainee (innovation in manufacturing of medicines) 18 June 2023 23:59 CET Trainee
Healthcare Data Science Specialist
Healthcare Data Science Specialist 21 June 2023 at 23.59 CET Temporary agent
21 June 2023 at 23.59 CET Temporary agent
Trainee (Analysing clinical trial data and structuring scientific documents) 18 June 2023 23:59 CET Trainee
Trainee (Enhancing medicines' benefit/risk information in women and in pregnancy) 18 June 2023 23:59 CET Trainee
Trainee (Establishing the value of RWD in regulatory applications for decision making) 18 June 2023 23:59 CET Trainee
Trainee (Pharmacovigilance)
Trainee (Pharmacovigilance) 18 June 2023 23:59 CET Trainee
18 June 2023 23:59 CET Trainee
Trainee (Review the utility of eHealth/mobile data and social media data) 18 June 2023 23:59 CET Trainee
Trainee (Better use of in vitro and in-silico tools to establish bioequivalence of complex generics) 18 June 2023 23:59 CET Trainee
Trainee (Regulatory Affairs)
Trainee (Regulatory Affairs) 18 June 2023 23:59 CET Trainee
18 June 2023 23:59 CET Trainee
Trainee (GMP and PV inspection programmes improvement) 18 June 2023 23:59 CET Trainee
Trainee (Inspections: Building Good Clinical Practice and bioequivalence inspection capacity) 18 June 2023 23:59 CET Trainee
Trainee (advanced therapies and oncology focusing on innovative medicines) 18 June 2023 23:59 CET Trainee
Trainee (EU Innovation and Development Enabler and Accelerator) 18 June 2023 23:59 CET Trainee
Trainee (Review of oncology and haematology products & maintenance of related scientific memory DB) 18 June 2023 23:59 CET Trainee
Trainee (guideline management tool)
Trainee (guideline management tool) 18 June 2023 23:59 CET Trainee
18 June 2023 23:59 CET Trainee
Trainee (Business Analysis & Forecasting)
Trainee (Business Analysis & Forecasting) 18 June 2023 23:59 CET Trainee
18 June 2023 23:59 CET Trainee
Trainee (The therapeutic potential of psychedelics - regulatory framework) 18 June 2023 23:59 CET Trainee
Trainee (Chemical, biological, radiological, nuclear threat database and guidance) 18 June 2023 23:59 CET Trainee
Trainee (Biostatistics and Clinical Trial Methodology and Implementation of the Estimands Guideline) 18 June 2023 23:59 CET Trainee
Trainee (Regulatory process management)
Trainee (Regulatory process management) 18 June 2023 23:59 CET Trainee
18 June 2023 23:59 CET Trainee

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.