Selection procedure reference: EMA/TR/11120
Deadline for applications: 30 September 2025 23:59 CET
The European Medicines Agency (EMA) is a decentralised agency of the European Union (EU), located in Amsterdam. It began operating in 1995. It is responsible for the scientific evaluation, supervision and safety monitoring of medicines in the EU.
This traineeship opportunity is now open for applications until 30 September 2025 23:59 CET, with an intake on 1 March 2026.
The Agency is looking for motivated, qualified recent graduates or students on an Erasmus+ or other programme or PhD students or Master's students (who posses a previous degree), who are interested in gaining experience and contribute to the Agency’s work for every patient in Europe. The purpose of a traineeship at the Agency is to perform tasks that are predominantly in the interest of the trainee’s training and principally serve to increase the trainee’s knowledge and to gain relevant experience.
We are looking for a trainee in the Public and Stakeholders Engagement Department within the Stakeholders and Communication Division.
During your traineeship, you will contribute to stakeholder engagement and communication and, support the sustainability of the network.
The selected trainee will have the opportunity to contribute to the following projects:
1. Support stakeholders’ contributions to the diverse activities of the Agency through the developemnet and implementation of a 'Training and Information Action Plan' to support stakeholders' interactions with regulatory authorities.
2. Contibute to better understanding of how patients not affiliated with organisations can find more comprehensive information about medicines leveraging information provided at national and EMA levels.
3. Investigate opportunities for visualisation for EMA’s medicines landing pages.
Through this traineeship, you will:
To be eligible for consideration for this placement, you are required to:
For criteria 1 and 2, you will be required to provide proof in the application form and at the interview stage. Failing to present these documents may result in the disqualification from the procedure.
In addition to the eligibility criteria, you will have:
• Previous experience in regulatory affairs, pharmaceutical legislation or stakeholders' engagement
• Communication skills (English writing and verbal)
• Experience working for public health or medicines regulatory agencies
• Experience in drafting, conducting and analysing surveys
• Experience creating communication materials, ideally videography and video editing, visual design
You will demonstrate the following behavioural competencies:
The traineeship is offered for 10 months (1 March 2026 – 31 December 2026) and takes place at the Agency’s premises in Amsterdam with possibility for teleworking up to 40% of working time from The Netherlands and occasional teleworking from outside The Netherlands. Traineeships are offered for either full-time or part-time (80% or 50%) if combined with university studies.
The Agency pays a monthly stipend of €1,963.93 for a full-time traineeship (reduced accordingly for 80% or 50%) and a travel contribution upon joining the Agency.
Each trainee will have a mentor at the Agency who will guide the trainee through the programme.
The conditions of employment are stated in the Executive Decision on rules governing the traineeship programme at the EMA available here.
Deadline for applications | 30 September 2025 23:59 CET |
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Assessments (remote) | From mid-October 2025 to mid-November 2025 |
Decision and offers | By end of November 2025 |
Placement start | 1 March 2026 |
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Domenico Scarlattilaan 6 - 1083 HS Amsterdam - The Netherlands
Telephone +31 (0)88 781 6000 - Email recruitment@ema.europa.eu
© European Medicines Agency, 2024. Reproduction is authorised provided the source is acknowledged.