Junior Project Manager

Are you an ambitious Junior Project Manager who likes to work in an European environment?  We are looking for a keen and talented colleague to coordinate on a country-level the implementation of a clinical trial.

About Ecraid
Established in January 2022, the European Clinical Research Alliance on Infectious Diseases (Ecraid) is an operational clinical research organisation dedicated to reducing the impact of infectious diseases on individual and population health. We focus on two main areas: Setting up and performing high quality clinical trials on infectious diseases and antimicrobial resistance and building a strong and unique academic clinical research network with broad European support.

Our Culture: Working at Ecraid
Ecraid is a purpose-driven, people-centred organisation that embraces academic excellence, diversity, and collaboration. We believe that the synergy of our talented individuals and continuous personal development is key to achieve outstanding results.
We have an international oriented work environment and our office language is English.
We support broad personal development and growth in the way we work and strive to make you multi-skilled so you can see and experience Ecraid from different perspectives.

Your role
As a Junior Project Manager, you will be responsible for the operational set up & execution of a clinical trial in 1-3 European countries, all within the applicable laws and regulations, ICH/GCP guidelines and SOPs. For example, you support in setting up a study by performing regulatory submissions of study documents, negotiating contracts with study sites and checking the quality of data produced by a study site. Quality is our top priority (''audit ready at all times''). You will be guided by a (senior) Project Manager.  Our large scale European projects are either financed from public funds or directly by pharmaceutical clients.

Who are you?
To succeed in this role, the following knowledge, skills and experience are required:

•        You have 0-3 years relevant operational experience (trial coordinator within a hospital, CRA/clinical trial administrator within a CRO or pharmaceutical company).

•        HBO/ Master degree towards Life sciences and/or Biomedical sciences

•        Experience in scientific clinical research

•        Knowledge of (inter)national laws and regulations, ICH  and GCP

•        Use of applications (such as EDC tools)

•        Excellent communication skills in English

•        You are already based in the Netherlands

You are enthusiastic, results-driven, decisive, and bright. You are quick to understand various research designs, you thrive in a fast-changing environment, and you find it rewarding to work in an international setting.

What we offer

We offer a challenging and meaningful job in an inspiring work environment in Utrecht, where you will be surrounded by intelligent, collaborative and enthusiastic colleagues. This position is offered on a temporary one-year employment contract, with the potential for extension. We offer a monthly gross salary of between € 3.764,20 and € 5.418,13 that commensurate with experience, based on a full-time workweek of 36 hours.
Beside this we offer:

•        13th month salary

•        Wellbeing at work via access to Open-Up

•        Company party’s and colleagues initiatives

•        Unlimited pay for public transport

•        Remote and flexible working

•        A Mac laptop and other professional tools to do your job successful

•        Commuting allowance: € 0.23 per kilometer

Interested in joining our mission?
Send us your resume together with your cover letter by pressing the apply button.

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