Preclinical Science and Operations lead (Oncology) - Human Health > Charleroi > Joboolo BE :
Company : Univercells Location : Charleroi Wallonia From : Talent BE
o Contingency planning. * Designs study operations and ensures appropriate documentation is prepared. * Ensures the viability of the analysis plan and contributes to planning and analysis. * Drives operational budgets and timelines * Represents vaccine development department as appropriate at internal and external meetings. * Drives high bioethical standards. * Ensures timely and effective communication with relevant stakeholders * Provides insight into operations in order to support strategic decision making * Ensures in vivo evaluations are designed to be operationally feasible and will provide provide accurate,meaningful data to inform decision making. * Produces project plans and, in collaboration with relevant stakeholders, drives projects to plan. * Ensures that GLP requirements for study related documentation are met. * Acts as subject matter expert on in vivo operations. * Ensures all studies are conducted to the highest bioethical standards….REQUIREMENTS & QUALIFICATIONS:
* Relevant academic qualification up to post graduate level (Masters in relevant science subjectpreferred).
Preclinicaloperations are in scope for this role:
post holders should be able todemonstrate appropriate qualifications and experience that credibly demonstrates their suitabilityfor the role. * At least 5 years industry or academic experience in a relevant role including oversight of preclinicaloperations. * Strong interest in the development of pharmaceutical interventions against infectious dieseases,especially those impacting Low and Middle Income countries (LMICs) and oncology field. * Direct experience on the design, conduct and analysis of preclinical (non-human) evaluation of medicinalproducts. * A good knowledge of epidemiology and relevant statistical methods, in particular infectious viruses andemerging pathogens. * Understanding of and direct experience with data analysis (supported by academic qualificationsand/or experience). * Demonstrated expertise in ethics * Experience in dealing with finance, budgeting and contracts, especially with contract research organizations. * Capability to oversee project management. * Experience and understanding of QA, QC and regulatory processes * Strong knowledge of pharmaceutical development, ideally in the area vaccines and oncology * Knowledge of GLP or GLP-trained or at least experience with Good Research Practices (GRP) for studydocumentation. * Good communication skills. * Effective collaborator. * Analytical skills. * Fluency in English absolutely required; additional languages useful, especially FR or NL. Univercells CharleroiWallonia
