Emploi Clinical trial Gand

 ...As we are growing, we are currently looking for a Clinical Trial Manager (CTM). The CTM is responsible for all operational aspects of the assigned clinical studies from monitoring initiation till closure of the studies. The successful candidate will have clinical trial... 

 ...Proclinical is seeking dedicated Clinical Project Managers to join a dynamic team in Belgium. This role is perfect for those who are passionate about managing clinical trials and have a keen interest in complex therapy areas. This is a global role, offering the opportunity... 

 ...Clinical Operations Development Lead page is loaded Clinical Operations Development Lead Apply locations Gent time type Full time...  ...Operations Development Leads (CODL) to strengthen the Global Clinical Trial Operations team. Ideally, location would be based in Belgium.... 

 ...to implementation, our unified Enterprise Imaging Platform is purpose-built to reduce complexity, improve productivity and deliver clinical value. We use our proven track record as an innovator, our in-depth medical knowledge and our strategic guidance to help... 

 ...support our growth, we are looking to strengthen our core team of consultants with a senior consultant with proven experience in clinical strategy & process improvement in hospitals. Your responsibilities As a  senior consultant , you are the link between  Hict... 

 ...through effective planning and implementation of territory key account plans. To meet all relevant standards as set by the company and Clinical Sales Manager Accountabilities To establish, maintain and develop positive relationships with partners local key opinion... 

Our client is an American Biomedical company that specializes in researching blood samples. With this research they try to develop medication for patients with long-term and chronic diseases. Since a few years the company is also located in Belgium, in Ghent. Through ...

 ...better and work smarter. We do this by offering products and services tailored ... **Your responsibilities include**: · - Oversee clinical trial billing process, coordinating with other departments and ensuring timely invoicing and financial setup. · - Generate and... 

 ...companies in an innovative way to help them achieving their (pre)clinical milestones timely. Our facilities are perfectly designed for...  ...up the quality of a variety of Drug Products used in clinical trials (capsules, tablets, solutions, suspensions, injectables, biologics... 

 ...immunogenicity assay development/validation for large molecules and/or clinical immunogenicity risk assessment and data interpretation....  ...commissioning of validation packages and bioanalysis of clinical trials by external bioanalytical vendors. Participate in vendor... 

 ...diverse statistical/programming tasks and resources , supporting the clinical development programs within argenx . Providing programming...  ...the statistical programming tasks for multiple clinical trials and integrated analyses (e.g., ISS, ISE). Good communication... 

 ...indication from initiation till closure of activities ensuring that clinical data completeness, accuracy and consistency meet the standards...  ...). Dependent on the program (phase and number of clinical trials) and the Line Management responsibilities, the DML may also act... 

 ...quality specialized laboratory and diagnostic solutions while leveraging patient data and scientific insight to shape and advance clinical trials. With our global footprint and access to leading regional labs, data, patients, technology, and partnered resources, we support... 

 ...evaluating, selecting, developing, and analytically validating clinical biomarker assays, primarily on ligand binding assay platforms....  ...study monitor, overseeing bioanalytical study phases of clinical trials, reviewing sample analysis plans and reports, and providing... 

 ...monitor corrective actions;  • Support development and execution of supply strategies for clinical studies;  • Prepare CMC sections to support timely submission of clinical trial applications;  • Develop SOPs effectively describing CMC processes;  • Liaise with... 

 ...record documentation of IMP batches and support release of IMP for clinical studies ensuring timelines are met Review of deviation...  ...excursions Support in compiling of submission dossiers for Clinical Trial Applications Provide strategic GMP guidance to third-party... 

 ...responsabilities include: Responsible for the completion of QC testing related to the manufacturing of autologous products for clinical trials and commercial operation in a controlled cGMP cleanroom environment. Ensure testing is completed in compliance with all... 

 ...exempt level position with responsibilities for performing QC testing related to the manufacturing of cell therapy products for clinical trials and commercial operations in a controlled GMP environment. Major Responsibilities: ... - Responsible for the... 

 ...quality specialized laboratory and diagnostic solutions while leveraging patient data and scientific insight to shape and advance clinical trials. With our global footprint and access to leading regional labs, data, patients, technology, and partnered resources, we support... 

 ...exempt level position with responsibilities for performing QC testing related to the manufacturing of cell therapy products for clinical trials and commercial operations in a controlled GMP environment. Major Responsibilities: - Responsible for the completion of...