Clinical Trial Associate II

Join Immatics and shape the future of cancer immunotherapy; one patient at a time!  

Immatics is committed to making a meaningful impact on the lives of patients with cancer. We are the global leader in precision targeting of PRAME, a target expressed in more than 50 cancers. Our cutting-edge science and robust clinical pipeline form the broadest PRAME franchise with the most PRAME indications and modalities, spanning TCR T-cell therapies and TCR bispecifics. 

Why Join Us? 

• Innovative Environment: Help to pioneer advancements in cancer immunotherapy. 

• Collaborative Culture: Be part of a diverse team dedicated to your professional growth. 

• Global Impact: Contribute to therapies that make a lasting impact on patients globally. 

We are seeking a Clinical Trial Associate II to support our US Clinical Operations team. The Clinical Trial Associate II will be responsible for Providing support for the GCP compliant clinical trial planning, conduct and oversight of clinical trials. 

FLSA Classification: Salary, Exempt  
Schedule: 8:00 AM – 5:00 PM; Monday to Friday 
Reports to: Associate Director, Team Lead Trial Management 
Location: Remote  

Salary Range: $80,000 - $100,000

What You’ll Do: 

Main responsibilities of this position include but are not limited to the following tasks:  

• Keeping oversight, incl. but not limited to: 

• tracking tools set-up and maintenance 

• report preparation 

• clinical trial documents preparation, performing review and/ or quality control 

• Providing support to the administration of clinical trials, incl. but not limited to: 

• meeting organization 

• preparation of meeting minutes 

• coordinating review processes and signature rounds 

• printing / arranging printing service 

• preparation of the Investigator Site File template  

• Organization of investigator grant payments and oversight of investigator grant payments 

• Development and maintenance of SOPs, guidance documents & training material 

• Minimal supervision required for routine tasks  

Required Experience and Education: 

• Bachelor's degree in a life science/medical field or equivalent experience 

• 2+ years working experience in the clinical research area in the pharmaceutical/biotech industry with ICH-GCP knowledge 

• Proactive contribution to development of team structure and processes 

• Demonstrated computer skills, including Microsoft Office and clinical trial systems (i.e., eTMF, CTMS). 

• Team-oriented and a strong team player 

• Ability to identify, analyze and communicate problems and suitable solutions  

• Independent, accurate and attention to detail working style 

• Good understanding of priorities within own scope, prioritization requires limited interaction with supervisor 

• High degree of initiative and intrinsic motivation to exceed basic expectations for own tasks and responsibilities