Clinical Research Associate II/Sr.

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 Research Associate II/Sr. to support our Clinical Operations. The Clinical Research Associate will be responsible for ensuring clinical trial site management and monitoring activities in compliance with GCP guidelines, national and local regulations or laws, and SOPs 

FLSA Classification: Salary, Exempt  

Schedule:  Monday - Friday; 8:00 am - 5:00 pm; preferred Western region of USA  

Department: Clinical Operations  

Reports to: Associate Director, Clinical Operations   

Supervisory responsibilities: No  

Location: Fully Remote 

What You’ll Do: 

As a Clinical Research Associate II/Sr., you will play a key role in supporting our Clinical operations:  

• Support clinical trial site feasibility and site selection process 

• Conduct all aspects of clinical monitoring for clinical trials including conduct of site qualification visits, site initiation visits, routine monitoring visits and close-out visits at clinical trial sites 

• Support the maintenance of the Investigator Site Files and sponsor Trial Master Files 

• Conduct all aspects of site management as prescribed in the clinical trial specific functional plans 

• Prepare accurate and timely trip visit reports 

• Review progress of clinical trials, especially patient recruitment and clinical trial data capture, and initiates appropriate actions to achieve objectives 

• Organize and make presentations at Investigator Meetings 

• Participate in the development of Case Report Forms and clinical trial documents 

• Act as primary contact for cli