You will be responsible for the overall administrative coordination of a Horizon Europe project and provide support in the acquisition of new projects.The scientific coordination of the project lies with the colleagues in FiBL Switzerland. Depending on the needs, you will provide support in preparing new project applications, or help with Grant Agreement Preparation of acquired projects.
Are you an experienced Clinical Research Associate (CRA) based in France with a strong background in medical device studies? We are seeking a dedicated professional to manage clinical monitoring activities across 4-5 investigator sites. This position offers excellent flexibility, requiring an average monthly resource commitment of 50-60% of a full-time role.As a Clinical Research Associate for this project, you will be responsible for end-to-end site
As a Corporate Business Controller, you will play a pivotal role in the financial management of the Business Unit. You act as the guardian of the structure cost performance (SG&A), bridging the gap between high-level financial strategy and operational execution. Your mission is to provide transparency, challenge the status quo, and drive cost-efficiency across the organization. You will operate in a complex, international matrix environment, collaborating
As a Business Analyst within the Facility & Purchase to Pay cluster, you will play a key role in ensuring business continuity and driving innovative improvements. Are you the expert who can translate complex requirements into seamless processes? Then this is your next challenge.Duration of project: asap - 30/04/2027Contract type: Consultancy or Freelance Work location: Brussels (minimum 50% on-site / 50% homeworking possible after the onboarding period)
Are you ready to elevate your career and manage world-class quality systems at DPDS Beerse? Join our team as a quality assurance specialist and drive compliance in a growth-oriented, supportive pharmaceutical environment.Job DescriptionAs our new quality assurance specialist, you play an essential role in optimizing our document and training workflows. You get to champion cGMP compliance while working alongside an empowering team that values your
3 june 2026
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