Senior Clinical Research Associate

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 Senior Clinical Research Associate 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 

Salary range: $120,000.00 - $125,000.00

What You’ll Do: 

As a Senior Clinical Research Associate, 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 clinical trial supplies and other suppliers (vendors) 

• Participate in regular clinical trial team meetings 

 Secondary Functions:  

• Mentor less experienced or new CRA colleagues 

• Perform CTM tasks as appropriate and as delegated by the CTM 

• Proactively contributes to continuous improvement of Clinical Operation specific processes, procedure and templates 

Required Experience and Education: 

• Min. 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) 

• In-depth knowledge of ICH-GCP, FDA and EMA and applicable local regulations and laws <