Patient Recruitment Coordinator, Clinical Research

**We are looking for a Clinical Data Coordinator for our client in the health sector based in Leuven.** **Job description**: **Responsibilities**: - Create and manage clinical trial databases, including data entry and quality control checks - Work with clinical research staff to collect and organize study data - Generate study reports and ensure accuracy...

At Terumo, we enhance lifesaving medical technologies for the benefit of society. Are you eager to contribute to people's health and patients' wellbeing? We'll challenge you to become a master in your field of expertise. You can invest your talents in balance with your personal aspirations - live and work in harmony. Built on our Japanese origins; we are...

50000 EUR - 50000 EUR - Leuven, Belgium - Permanent **Study Start Up & Regulatory Coordinator - Global CRO - Hybrid - Leuven, Belgium** I am currently working alongside my client, a global CRO with a long and rich history within Clinical Research, to support them in their search for a Study Start Up & Regulatory Submissions Coordinator to join their...

Job Summary: Our corporate activities are growing rapidly, and we are currently seeking a full-time, office-based **eClinical Coordinator** to join our Data Management team. By working with the eClinical Project Manager and other team members, these professionals ensure the accuracy of data that is reported by patients for clinical studies. If you are...

Overview Medpace is a full-service clinical contract research organization (CRO). We provide Phase I-IV clinical development services to the biotechnology, pharmaceutical and medical device industries. Our mission is to accelerate the global development of safe and effective medical therapeutics through its scientific and disciplined approach. We...

Job Summary Are you ready to make a significant impact in the world of healthcare? Join our team as a Clinical Trial Assistant and play a pivotal role in advancing medical research. Reporting to the Clinical Operations Manager, Irene Barriocanal, you will be an essential part of our dynamic European Medical and Clinical Division at the EMEA HQ. ...

Solliciteren kan tem 02/06/2024 **Verleg grenzen als coördinator clinical research unit voor kinderen (Petit-CRU)**: De dienst kindergeneeskunde van UZ Leuven, samen met andere diensten betrokken bij de zorg voor zieke kinderen, heeft een belangrijke taak om nieuwe behandelingen voor de pediatrische patiëntengroep te ontwikkelen en te implementeren. Om...

Job Summary: We are seeking a full-time, office-based Fleet Coordinator to join our team in Leuven within a permanent contract. If you want an exciting career where you use your previous expertise in Facilities and have a strong desire to develop and grow your career even further, then this is the opportunity for you. Responsibilities: - The Fleet...

You hold a PhD degree relevant for (bio)medical sciences. If you have recently obtained your PhD, it is important that you support your research and growth potential with academic references (e.g. demonstrate potential through at least one top publication, academic references, promising research projects and articles in preparation).You have an strong...

Solliciteren kan tem 02/06/2024 Verleg grenzen als coördinator clinical research unit voor kinderen (Petit-CRU) De dienst kindergeneeskunde van UZ Leuven, samen met andere diensten betrokken bij de zorg voor zieke kinderen, heeft een belangrijke taak om nieuwe behandelingen voor de pediatrische patiëntengroep te ontwikkelen en te implementeren. Om...

Company Description PSI is a leading Contract Research Organization with more than 25 years in the industry, offering a perfect balance between stability and innovation to both clients and employees. We focus on delivering quality and on-time services across a variety of therapeutic indications. **Job Description**: PSI **Medical Monitors **provide medical...

We are looking for a highly motivated, enthusiastic, critical, and creative person with a master degree or equivalent in a relevant field, such as Medicine, Biomedical Sciences, Bioscience Engineering, Biomedical Engineering, Biochemistry, Biology (or will obtain this degree in 2024)Solid knowledge of molecular biologyPrior experience with general laboratory...

PhD in biomedical sciences, bioengineering, biotechnology, pharmaceutical sciences, nutrition or related fieldStrong interest in fundamental mechanisms of diseaseGood academic performance at MSc and PhD levelPublished articles as first authorProficiency in written and spoken EnglishCreative with a strong interest in innovationAble to integrate in an...

- An excellent curriculum with a Master’s degree in biomedical sciences or in biology, biotechnology, bio-engineering, medicine or pharmacy. - Highly motivated to study the immunology and metabolism of malaria, a major tropical infectious disease.- Eligibility and suitable profile for application for a fellowship (e.g. FWO) is an important asset.- Felasa B...

Are you an experienced Clinical Research Associate looking for a new challenge? We are a mid-sised CRO looking for a CRA II - Senior CRA to join our team in Belgium. This is a home-based role with 80% travel across the whole of Belgium, working on multi-sponsor clinical trials across all therapeutic areas. As a CRA II - Senior CRA, you will be responsible...

**Bioinformatics Postdoctoral Scientist on an EU-funded project**: - Employer- KU Leuven- Location- Leuven- Salary- nvt- Closing date- 1 Apr 2024- Discipline Computing, Health Science Job Type PhD Studentship Employment - Hours Full time Duration Fixed term Qualification Masters Sector Academia- You need to sign in or create an account to a...

Job Summary: Our corporate activities are growing rapidly, and we are currently seeking a full-time, office-based ** eClinical Project Manager** to join our Data Management team. This role will work with both local and international teams and will manage global studies. If you want an exciting career where you use your previous expertise and can develop and...

Overview Medpace is a full-service clinical contract research organization (CRO). We provide Phase I-IV clinical development services to the biotechnology, pharmaceutical and medical device industries. Our mission is to accelerate the global development of safe and effective medical therapeutics through its scientific and disciplined approach. We...

Overview Medpace is a full-service clinical contract research organization (CRO). We provide Phase I-IV clinical development services to the biotechnology, pharmaceutical and medical device industries. Our mission is to accelerate the global development of safe and effective medical therapeutics through its scientific and disciplined approach. We...

Job Summary: Responsibilities: - Monitor laboratory operations in order to verify that accurate, precise, and reliable data are being generated for clinical trials; - Interact with corporate leadership, scientific liaison, project management, administration, government agencies, accrediting agencies, and potential sponsors/clients to gain information and...