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Trainee (Supporting stakeholders' engagement and medicines health information)
The trainee will support stakeholder engagement processes and investigate how public enquiries are handled across the European medicines regulatory network. Responsibilities include developing data collection templates, conducting surveys, and preparing reports with practical recommendations to improve coordination.
Requirements
Candidates must hold or be pursuing a university degree in biomedical sciences, public health, or social sciences. Applicants must possess a C1 level of English and a B2 level in another official EU language.
Full job description
Selection procedure reference: EMA/TR/11533
Deadline for applications: 30 September 2026 23:59 CEST
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 2026 23:59 CEST, with an intake on 1 March 2027.
About the traineeship programme
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 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.
Placement description
The Public and Stakeholders Engagement Department is seeking a motivated trainee to support improvements of its stakeholders’ engagement processes and to investigate how public enquiries are handled across the European medicines regulatory network.
Specific objectives and projects
For its stakeholder engagement activities, EMA operates within established frameworks that guide engagement and communication with key stakeholder groups, including patients and consumers, healthcare professionals, academia, and industry.
This traineeship offers a unique opportunity to contribute to enhance how the Agency organises and communicates information, providing stakeholders with a clear, accessible and strategic overview of its activities.
The project on stakeholder engagement reporting will be expected to:
• Develop a standardised data collection template including minimum required data fields. • Propose a streamlined process for collecting inputs across the Agency offices (including options for digital tools). • Propose a revised report format that is more concise, structured, and reader-friendly (including visual elements).
The project examining public enquiries will involve engaging with representatives from national competent authorities to collect information on their systems, processes and experiences in managing public queries.
The trainee will be expected to:
• Develop and conduct a survey of relevant stakeholders within the EU regulatory network. • Analyse information on communication channels, workflows, response timelines, query types and volumes. • Identify similarities, differences and examples of good practice across Member States. • Explore how queries are currently redirected between EMA and national authorities and identify potential inefficiencies or areas for improvement. • Assess the use of digital solutions and artificial intelligence in public query handling. • Prepare a report summarising findings and proposing practical recommendations to strengthen collaboration and coordination across the network.
Learning outcomes
The trainee is expected to:
• Learn about EMA’s frameworks and approach to stakeholder engagement. • Gain hands-on experience in process optimisation within a European regulatory environment. • Develop skills in data structuring, reporting, and professional communication. • Gain understanding of factors contributing to effective communication and engagement. • Gain knowledge of the Agency’s processes and regulatory work. • Gain insight into how EMA and national competent authorities interact with patients, healthcare professionals and the public. • Develop skills in survey design, stakeholder engagement and qualitative data analysis. • Gain experience in mapping processes across multinational organisations.
Eligibility criteria
To be eligible for consideration for this placement, you are required to:
enjoy full rights as a citizen of a European Union Member State or Iceland, Lichtenstein and Norway;
possess a relevant university degree (minimum of three years or more) in biomedical sciences (e.g. pharmacy, medicine) or public health or social sciences, that must have been obtained between 30 September 2025 and 30 September 2026 or be a university student on an Erasmus + or a similar programme or a PhD student or a Master's student with a previous fully finished degree in the areas mentioned before.
a thorough knowledge of English (at least level C1) and good knowledge of other official EU language (at least B2) of the Common European Framework for Languages
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.
Additional skills
• Experience in project management • Experience in stakeholder engagement and/or communication • Experience with process improvement • Strong analytical and organisational skills • Ability to synthesise information clearly and concisely • Excellent written communication skills in English
Behavioural Competencies
You will demonstrate the following behavioural competencies:
Communication skills
Interpersonal skills
Working with others
Adaptability
Research and analytical skills
Learning and development
Conditions of traineeship
The traineeship is offered for 10 months (1 March 2027 – 31 December 2027) 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 €2,049.77 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.
Expected selection timelines
Deadline for applications
30 September 2026 23:59 CEST
Assessments (remote)
From mid-October 2026 to mid-November 2026
Decision and offers
By end of December 2026
Placement start
1 March 2027
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Domenico Scarlattilaan 6 - 1083 HS Amsterdam - The Netherlands
The mission of EMA is to foster scientific excellence in the evaluation and supervision of medicines in the EU.
Industry
Government Administration
Company size
501-1,000 employees
Founded
1995
Headquarters
Amsterdam, North Holland
LinkedIn followers
376,424
The European Medicines Agency (EMA) is a decentralised body of the European Union with headquarters in Amsterdam. Its main responsibility is the protection and promotion of public and animal health, through the evaluation and supervision of medicines for human and veterinary use.
Offices: Domenico Scarlattilaan 6, Amsterdam, North Holland 1083, NL
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