Senior Clinical Sciences Manager

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. 

Role Overview 

We are seeking a Senior Clinical Sciences Manager to support the execution of our clinical trials, including the SUPRAME (IMA203-301) study. The Senior Manager will be responsible for supporting patient journey navigation, primarily for U.S. sites, and updating patient-facing and clinical trial materials. In addition, this role will contribute to protocol development, conduct literature research, support trial outcome reporting, and deliver training to internal and external stakeholders. 

  
Reports to: Director, Clinical Sciences 
Location: Fully Remote 

Salary Range: $155,000 – 175,000 

Basic Qualifications: 

• Bachelor’s degree in biology, pharmacy, or a related scientific field  

• 7+ years of experience conducting literature research using clinical and medical databases  

• Demonstrated experience supporting clinical trial activities, including protocol and patient-facing materials  

• Experience training site staff or internal teams on clinical trial protocols and materials 

Preferred Qualifications:

• Master’s degree in biology, pharmacy, or a related scientific field  

• Experience supporting regulatory documentation (e.g., IRB submissions, RFIs)  

• Experience working in oncology or cell therapy clinical development  

• Advanced ability to translate complex scientific data into clear, actionable insights and presentations  

• Experience working cross-functionally in a global clinical trial environment 

In this role