
201 - 500 employees
Founded 2000
đ§Ź Biotechnology
đ Pharmaceuticals
đŹ Science
Biotechnology ⢠Pharmaceuticals ⢠Science
Immatics is a biotechnology company focused on developing targeted immunotherapies for cancer patients, particularly in treating solid tumors. The company combines the discovery of cancer immunotherapy targets with the development of specific T cell receptors to enable a robust immune response. Immatics' pipeline includes Adoptive Cell Therapies and TCR Bispecifics, and it collaborates with global leaders in the pharmaceutical industry. The company's mission is to advance its therapies to improve the lives of cancer patients, and it maintains a strong commitment to innovation in immunotherapy technologies.
đĽ 3 minutes ago
đŁď¸đŠđŞ German Required
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201 - 500 employees
Founded 2000
đ§Ź Biotechnology
đ Pharmaceuticals
đŹ Science
Biotechnology ⢠Pharmaceuticals ⢠Science
Immatics is a biotechnology company focused on developing targeted immunotherapies for cancer patients, particularly in treating solid tumors. The company combines the discovery of cancer immunotherapy targets with the development of specific T cell receptors to enable a robust immune response. Immatics' pipeline includes Adoptive Cell Therapies and TCR Bispecifics, and it collaborates with global leaders in the pharmaceutical industry. The company's mission is to advance its therapies to improve the lives of cancer patients, and it maintains a strong commitment to innovation in immunotherapy technologies.
⢠Ensure clinical trial site management and monitoring activities in compliance with GCP guidelines, applicable regulations, and SOPs ⢠Execute clinical monitoring activities, including qualification, initiation, routine monitoring, and close-out visits ⢠Maintain Investigator Site Files and Trial Master Files ⢠Implement site management activities in line with trial-specific functional plans ⢠Prepare accurate and timely visit reports ⢠Review trial progress (e.g., patient recruitment, data capture, issue resolution) and initiate appropriate actions ⢠Serve as primary contact for clinical trial supplies and other stakeholders or vendors ⢠Participate in clinical trial team, department and company meetings ⢠Contribute to the development of trial specific documents ⢠Contribute to the continuous improvement of Clinical Operations processes and procedures
⢠Bachelorâs degree in life sciences, nursing, or a comparable field ⢠2+ years of experience in on-site monitoring (all visit types) within the pharmaceutical or biotechnology industry ⢠In-depth knowledge of ICH-GCP, applicable regulations, and clinical trial systems (e.g., eTMF, CTMS, EDC, IRT) ⢠Basic knowledge of oncology, including terminology and underlying science, is preferred ⢠Excellent presentation and communication skills in German and English (minimum C1 level) ⢠Willingness to travel up to 50-75%
⢠job bike ⢠job ticket ⢠Health Programs ⢠childcare benefits ⢠relocation allowance ⢠Company summer and winter events
Apply Nowđ May 13
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