Preclinical Project Manager (80-100%)

h3Preclinical Project Manager (80-100%) /h3 pLimmaTech Biologics AG, a wholly owned subsidiary of Eli Lilly and Company, is a Swiss clinical stage biopharmaceutical company. We are advancing our vaccine pipeline to halt the increasing threat of global infections due to emerging antimicrobial resistance (AMR) and sexually transmitted diseases. Working at LimmaTech is a unique chance to be part of the development of life saving vaccines. /p pAre you excited about the opportunity to contribute to the development of early- to mid-stage vaccines by managing non-clinical studies and coordinating internal and external partners? Would you like to be part of a team translating preclinical data into well-planned development activities and high-quality documentation? /p pPreclinical Project Manager (80-100%) /p pto coordinate non-clinical studies and support vaccine development from planning through reporting. /p h3Your responsibilities /h3 pIn this role, you will: /p ul liManage non-clinical research and GLP studies with internal teams, external collaborators, and contract research organizations (CROs) to support research and clinical development activities. /li liPlan, coordinate, and track preclinical projects, including timelines, budgets, risks, deliverables, and dependencies. /li liAnalyze, interpret, and present preclinical data generated through immunological and functional assays such as ELISA, OPA, SBA, and multiplex immunoassays. /li liPrepare preclinical documentation, including protocols, study reports, toxicology reports, and contributions to regulatory documents. /li liCoordinate communication and study activities with external providers and internal stakeholders across functions. /li liOrganize study logistics, including materials, sample management, and shipments for in vivo and in vitro studies. /li liMaintain preclinical databases, inventories, and study materials to ensure data integrity and traceability. /li liSupport assay development, troubleshooting, and continuous improvement activities as needed. /li liEnsure compliance with applicable vaccine regulatory requirements, quality standards, and standard operating procedures (SOPs). /li /ul h3What we are looking for /h3 pYou are a proactive, flexible, and solution-oriented project manager who combines scientific understanding with strong organizational skills. You take ownership of timelines and deliverables, communicate effectively with internal and external partners, and remain focused on quality when managing competing priorities. /p h3Ideally, you bring: /h3 ul liA Master's degree in biology, microbiology, immunology, toxicology, or a related life sciences field. /li liA minimum of 3-5 years of relevant experience in preclinical research, project management, or drug or vaccine development. /li liExperience managing outsourced studies and working with CROs and external scientific partners in vaccine development. /li liExperience with immunological and functional assays, including ELISA, OPA, SBA, and multiplex immunoassays. /li liStrong experience in scientific data analysis, interpretation, and reporting. /li liFamiliarity with regulatory requirements applicable to non-clinical and GLP studies in vaccine development. /li liStrong project management, organizational, analytical, and problem-solving skills, with the ability to manage multiple projects and meet timelines in a fast-paced environment. /li liThe ability to work independently and collaboratively within cross-functional teams, with a high level of attention to detail and commitment to quality. /li liExcellent written and verbal communication skills in English and very good knowledge of Microsoft 365 applications, particularly Excel, as well as GraphPad Prism. /li /ul pThe working place is in Schlieren near Zürich, easily accessible by public transportation. If you meet the requirements of this exciting position and want to work in a friendly, highly motivated and dynamic team, we are interested in hearing from you. /p pDue to visa regulations, only applicants eligible to a Swiss work permit can be considered for this position. /p h3Job details /h3 ul libWork location /b 8952 Schlieren (ZH) /li libWorkload /b 80% - 100% /li libEmployment start /b By agreement /li libEmployment duration /b Permanent /li libQualification /b skilled /li libWork experience /b More than 3 years /li libEducation /b Master’s degree from a university or equivalent /li libEnglish /b Orally : Good knowledge Written : Good knowledge /li /ul #J-18808-Ljbffr