Immatics
201 - 500 employees
Founded 2000
𧏠Biotechnology
đ Pharmaceuticals
đŹ Science
Biotechnology âą Pharmaceuticals âą 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.
Freelance Clinical Research Associate, CRA
đ„ 3 minutes ago
đŁïžđ©đȘ German Required
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Immatics
201 - 500 employees
Founded 2000
𧏠Biotechnology
đ Pharmaceuticals
đŹ Science
Biotechnology âą Pharmaceuticals âą 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.
đ Description
âą Support clinical trial site management and monitoring activities âą Perform and support on-site monitoring visits âą Support the maintenance and updating of trial-specific tracking tools âą Collect site-specific clinical trial documents âą Support Trial Master File filing activities and TMF completeness checks âą Contribute to clinical trial site management and engagement âą Review patient recruitment progress and clinical data capture
đŻ Requirements
âą Degree in life sciences, nursing, medicine, pharmacy, or comparable field âą Solid experience as a Clinical Research Associate in pharmaceutical, biotechnology, or CRO environment âą Experience in on-site monitoring and Source Data Verification âą In-depth knowledge of ICH-GCP and applicable regulatory requirements âą Familiarity with clinical trial systems such as eTMF, CTMS, EDC, and IRT âą Experience in oncology clinical trials preferred âą Excellent communication skills in German and English âą Willingness to travel regularly within Germany
đïž Benefits
âą Flexible work arrangements âą Professional development opportunities
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