Clinical Trial Manager

2 days ago

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Immatics

Discovery of HLA-restricted tumor-associated peptides as cancer targets • Biomarkers • Immunomonitoring • Peptidomics & mass spectrometry • Standardized PBMC collection

201 - 500

Description

• Ensure clinical trial site management and monitoring activities in compliance with GCP guidelines, national and local regulations or laws, and SOPs for assigned clinical trials. • Conduct clinical trial site feasibility and selection. • Create, maintain and implement trial-specific plans, tools and documents required per SOP. • Oversee or perform collection of clinical trial site specific documents ensuring on time regulatory submissions.

Requirements

• Bachelor’s degree preferably in life science or nursing, or equivalent. • At least 4 years of on-site monitoring experience in the pharmaceutical/biotechnology industry (incl. all monitoring visit types). • Comprehensive knowledge of ICH-GCP, FDA and EMA guidelines and applicable local regulations. • Significant insights into clinical trial management activities. • Knowledge of basic medical oncology terminology and cell therapy is an advantage. • High degree of independent working, analytical thinking and excellent communication skills in German and English. • Good team player with very good organization, negotiation and resolution skills. • Willingness to travel up to 30%.

Benefits

• job bike • job ticket • Health Programs • childcare benefits • relocation allowance • Company summer and winter events

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