Immatics
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.
Discovery of HLA-restricted tumor-associated peptides as cancer targets • Biomarkers • Immunomonitoring • Peptidomics & mass spectrometry • Standardized PBMC collection
Clinical Research Associate - Senior
September 15, 2024
Immatics
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.
Discovery of HLA-restricted tumor-associated peptides as cancer targets • Biomarkers • Immunomonitoring • Peptidomics & mass spectrometry • Standardized PBMC collection
📋 Description
• Responsible for the clinical monitoring activities for assigned clinical trial sites. • Conduct all aspects of clinical monitoring for clinical trials including site visits for qualification, initiation, routine monitoring and close-out. • Review progress of clinical trials and initiate appropriate actions to achieve objectives. • Support the maintenance of the Investigator Site Files and Trial Master Files. • Prepare accurate and timely monitoring visit reports.
🎯 Requirements
• Bachelor’s degree preferably in life science or nursing, or comparable education. • 5 - 7 years of on-site monitoring experience in the pharmaceutical/biotechnology industry. • Understanding of medical oncology terminology and science. • Excellent communication and interpersonal skills. • Strong organizational skills, with the ability to manage multiple projects and meet deadlines. • In-depth knowledge of ICH-GCP, FDA, EMA and applicable local regulations and laws. • Valid Driver’s license. • Demonstrated computer skills, including Microsoft Office and clinical trial systems (i.e., eTMF, CTMS).
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