Clinical Enrolment Manager Belgium

Job Summary: We are seeking a **Manager, Clinical Packaging and Supplies** to organize and execute activities involved with the management of investigational product and associated ancillary supplies in support of clinical studies. Are you interested in delivering effective, end-to-end collaboration, and training around the globe to accelerate the global...

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...

Job Summary: Medpace is the leading CRO for Biotech companies and is continuing to add Clinical Trial Managers of different experience levels to join our Clinical Trial Management Group in Belgium, Leuven. Clinical Trial Managers with expertise in Oncology/Cardiovascular/Endocrine/Metabolic are welcome to continue to work in their area of expertise or to...

Belgium (HQ) Quality The Position Materialise is a dynamic, high-tech company headquartered in Belgium, with offices worldwide. Founded in 1990, today we have over 2,300 employees around the globe. Materialise’s mission is to innovate for a better and healthier world through our software and hardware infrastructure and in-depth knowledge of additive...

Clinical Data Manager | Full Time | Healthcare | Leuven | 1091297 **Your responsibilities as a Clinical Data Manager**: - Develop and review data management procedures for clinical trials with sponsor companies and other departments; - Design reports and metrics that are useful management tools for your projects - Lead the design and validation of the CRF...

Job Summary: We are currently seeking a full-time, office-based Patient Recruitment Coordinator to join our growing Patient Recruitment team. This position will work on a team to accomplish tasks and projects that are instrumental to the company’s success. If you want an exciting career where you use your previous expertise and can develop and grow your...

Are you currently working in a CRO and looking to move your career forward to Regulatory Affairs ? This is a chance to do so. We are in search of a Regulatory Submissions Manager based in Leuven, Belgium to support this quality multinational CRO's daily operations. The company is focused on hiring the most talented people and are offering a lot of support in...

**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...

Job Summary: Our clinical activities are growing rapidly in Belgium, and we are currently seeking a full-time Project Coordinator to join our Clinical Operations team. This position will work on a team to accomplish tasks and projects that are instrumental to the company’s success. If you want an exciting career where you use your previous expertise and...

Experienced Clinical Database Programmer My Client who is a very successful, mid-size CRO are currently looking for an Experienced Clinical Database Programmer to join their team on a Hybrid bases in one of three locations; Leuven(Belgium), Milan(Italy) or Rotterdam(Netherlands). They are constantly growing, which allows for your personal growth as well as...

Job Summary: - Our clinical activities are growing rapidly, and we are currently seeking a full-time Site Relationship Coordinator to join our vibrant Clinical Operations team. This is a fantastic opportunity to work on pre-award and post-award study feasibilities, build and maintain strategic relationships with our network of sites, and develop key...

Company Description We are the company that cares - for our staff, for our clients, for our partners and for the quality of the work we do. A dynamic, global company founded in 1995, we bring together more than 2,300 driven, dedicated and passionate individuals. We work on the frontline of medical science, changing lives, and bringing new medicines to those...

**Junior Clinical Trial Assistant**: - Location: Leuven - Contact: Aurore Munaut - Job type: Contract - Contact phone: +32 10 68 53 31 - Industry: Pharmaceutical As a Junior Clinical Trial Assistant you will be the key support to clinical research projects, streamlining communication, maintaining systems and managing documents &...

Job Summary: Responsibilities: - Communicate and collaborate on global study activities; working closely with the project coordinator and clinical trial manager - Ensure timely delivery of recurrent tasks consistently with a high degree of accuracy - Compile and maintain project-specific status reports within the clinical trial management system - Interact...

Clinical Database Programmer | Full-time | Healthcare | Leuven | 1091299 **Your responsibilities as a Clinical Database Programmer**: - Setup, validate, and maintain study database systems in ClinTrak Lab; - Program edit checks, result reports, and label/tube type templates; - Program billing requirements within ClinTrak Lab; - Ensure programming study...

Oncacare - Global Oncology Site Network Patient Recruitment and Centricity Officer Full Time, Permanent Location: Brussels, Belgium Home based Able to travel at short notice - UK and Europe Introduction Are you looking for an outstanding opportunity to develop your career with ICON’s leading edge Global Commercial Oncology Site Network which is...

Job Summary: Responsibilities: **QEM Program activities** - Oversee and administer the QEM Program through maintaining Controlled Documents, Guidelines, Templates and associated training for Medpace staff - Develop and maintain a proficient, user-friendly QEM system - Provide training to QERM Office team members i.e., Clinical Quality and Risk Management...

Job Summary: Responsibilities: **QEM Program activities** - Oversee and administer the QEM Program through maintaining Controlled Documents, Guidelines, Templates and associated training for Medpace staff - Develop and maintain a proficient, user-friendly QEM system - Provide training to QERM Office team members i.e. Clinical Quality and Risk Management...

**The Job’s mission**: **Have you always wanted to work for one of the world's best employers within medical technology and an award-winning Great Place to Work Belgium?** For our innovative Mako robotics system, we are looking for a **Hybrid** **Clinical (Mako) Support Specialist** to cover the regions of **Antwerpen, Vlaams-Brabant & Limburg **in...

Company Description We are the company that cares - for our staff, for our clients, for our partners and for the quality of the work we do. A dynamic, global company founded in 1995, we bring together more than 2,200 driven, dedicated and passionate individuals. We work on the front-line of medical science, changing lives, and bringing new medicines to...