Associate Director - Clinical Operations

September 15

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Immatics

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

201 - 500

Description

• Global Clinical Trial Oversight. • Provide oversight on feasibility analysis, clinical trial site selection, qualification and initiation of new clinical trial sites and contracting with clinical trial sites in USA. • Provides clinical monitoring strategy and oversight in USA. • Maintains expert-level current knowledge of GCP industry trends and “current-thinking”. • Resource planning and onboarding for internal Clinical Research Associates, Clinical Trial Manager and Site Operations Leads in USA. • Ensure appropriate line management and employee development for internal Clinical Research Associates, Clinical Trial Managers and Site Operations Leads in USA. • Provides oversight on all Immatics clinical trial site related activities, incl. clinical monitoring activities and site operations in USA. • Provides oversight of clinical trial site feasibility/ selection in USA. • Provides oversight of qualification and initiation of new clinical trial sites in USA. • Ensures quality and adherence to relevant Standard Operating Procedures/Work Instructions (SOP/WI) and compliance with guidelines and ICH GCP.

Requirements

• Min. Master’s Degree, preferably in life science or nursing; or equivalent • At least 2 years of working experience as a Clinical Research Associate • At least 4 years of Clinical Monitoring experience (as Clinical Research Associate and Clinical Trial Manager) in the pharmaceutical / biotechnology industry, preferred in oncology and cell therapy • 1 - 2 years line management experience • Proactively driving high quality and efficiency to meet timelines and milestones • Main driver of innovation and development in own area • High degree of flexibility in an environment which is marked by a constant striving for excellence